Medical device company profile

VB Spine

Spinal implants, orthobiologics and enabling technologies built around an acquired spine-care portfolio.

Medical Device ManufacturerOrthopedics & MusculoskeletalSpineCommercial-stage

Headquarters🇺🇸Leesburg, Virginia, United States

Founded2025

Commercial statusCommercially availableSelected products commercially offered; availability and indications vary by product and market.

EmployeesNot confirmed

Estimated revenueNot confirmed

Disclosed fundingUS$5 million ^[190]Holding-company equity sold · Apr 2026

Official websitewww.vbspineco.com ↗

Company overview

VB Spine supplies implants, orthobiologics and enabling technologies for spinal surgery. The company was formed in April 2025 following the acquisition of Stryker’s U.S. spinal implants business by Viscogliosi Brothers.

Its portfolio includes the Vulcan spinal fixation system and acquired xvision spine-navigation rights. A February 2026 FDA decision for Vulcan names K2M, Inc. as applicant; the profile preserves that legal identity instead of rewriting the historical record under the VB Spine brand.

Anthony, John and Marc Viscogliosi serve as co-CEOs. Corporate headquarters are in Leesburg, Virginia, with a global manufacturing headquarters in Cestas, France. Portfolio integration, surgeon support and a global commercial organization underpin the company’s current operating model.

^{[178][179][180][181][182][183][184][185][186][187][188][190][192][194][195][196]}

Leadership

6 people

Anthony G. ViscogliosiCo-CEO ^[192]

John J. ViscogliosiCo-CEO ^[192]

Marc R. ViscogliosiCo-CEO ^[192]

Josh JohnsonGlobal President ^[192]

Thomas OglesbyChief Financial Officer ^[192]

Rick KovachChief Operating Officer ^[192]

Products & regulatory status How does MedTechIndex get this information?

Summary

VB Spine’s selected portfolio includes Vulcan and the acquired xvision platform. The audit also records the inherited K2M spine-device history, retaining original applicants and pre-acquisition dates. Current corporate ownership and the exact scope of older models are separate questions; the snapshot remains a selection rather than a full acquired-product catalog. ^{[192][196][195][130][129][180][182][1]}

The matched FDA history contains 12 distinct recall events: 2 open, 10 terminated. 2 were initiated during the five years beginning October 20, 2021; older open events are also retained. Z-1307-2022 (2022-06-13; open, classified): Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response; adverse local tissue reactions may occur related to cytotoxicity… Z-0705-2022 (2022-01-13; open, classified): Stryker received two (2) complaints for units from specific lots of Inner and Outer Dilators not fitting together properly during a surgical procedure. Some dilators from these lots and from other lots were subsequently determined to be affected by a manufacturing nonconformance. ^{[175][173][174]}

Regulatory snapshot How to read this snapshot

U.S. FDA

1
510(k) clearances: 0
De Novo grants: 0
PMA approvals: 0
Recall events

Latest recorded source review: 2026-10-20.

View 2 documented open recall events

Includes open events outside the mapped current portfolio; those events are excluded from the snapshot count.

Documented open FDA recall events
Recalled product / record	Initiated	Source
Yukon Straight Rod 4.0 x120mmZ-1307-2022	June 13, 2022	^[175]
Everest MI XT Inner DilatorZ-0705-2022 Everest MI XT Outer DilatorZ-0706-2022	January 13, 2022	^[173][174]

Commercial portfolio snapshot

Documented commercial product families.

Posterior spinal fixation

Vulcan Spinal System ↗

Multi-component posterior spinal fixation system for fusion procedures. ^[194][189]

FDA-cleared

Commercially offered; exact model and country availability should be confirmed with the manufacturer.

Augmented-reality spine navigation

xvision Spine System ↗

Acquired exclusive rights to the spine-navigation platform from Augmedics. ^[195]

Marketed · regulatory scope varies

Commercially offered; exact model and country availability should be confirmed with the manufacturer.

Activity & Milestones

2 events

2026-04-13 · Corporate

xvision spine rights acquisition completed

VB Spine completed acquisition of exclusive rights to the xvision Spine System from Augmedics. ^[195]

2025-04-01 · Corporate

Spine business acquisition completed

Formation followed acquisition of the U.S. spinal implants business from Stryker. ^[196]

196 Cited Sources

Accessed 10/29/2026

[1] FDA 510(k) database — research search ↗FDA / openFDA · regulatory record

[2] FDA K023703 — BI-OSTETIC ↗U.S. Food and Drug Administration · regulatory record

[3] FDA K042635 — DENALI SPINE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[4] FDA K051454 — ALEUTIAN SPACER SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[5] FDA K051531 — TECTONIC CERVICAL PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[6] FDA K052398 — MESA SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[7] FDA K052404 — DENALI DEFORMITY SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[8] FDA K060442 — PYRENEES CERVICAL PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[9] FDA K063399 — ALEUTIAN SPACER SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[10] FDA K063544 — MODIFICATION TO PYRENEES CERVICAL PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[11] FDA K070229 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[12] FDA K072914 — NATURAL BRIDGE LP TRANSVERSE CONNECTORS ↗U.S. Food and Drug Administration · regulatory record

[13] FDA K080024 — ALEUTIAN SPACER, MODEL K2-07-1004-01, K2-07-1005-01 ↗U.S. Food and Drug Administration · regulatory record

[14] FDA K080302 — CAYMAN BUTTRESS PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[15] FDA K080611 — MESA SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[16] FDA K080792 — K2M COCR ROD ↗U.S. Food and Drug Administration · regulatory record

[17] FDA K081107 — CASPIAN SPINAL SYSTEM, SCREWS, RODS, HOOKS, ROD CONNECTORS ↗U.S. Food and Drug Administration · regulatory record

[18] FDA K081380 — THORACOLUMBAR, LUMBAR AND SACRAL PLATES AND 6.0 AND 7.0 MM BONE SCREWS ↗U.S. Food and Drug Administration · regulatory record

[19] FDA K081381 — RANGE SPINAL SYSTEM, LARGE DENALI SCREWS ↗U.S. Food and Drug Administration · regulatory record

[20] FDA K082698 — ALEUTIAN IBF SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[21] FDA K082769 — MESA AND RANGE SPINAL SYSTEMS ↗U.S. Food and Drug Administration · regulatory record

[22] FDA K091253 — THORACOLUMBAR PLATE, MODEL 1208-41FXX, LUMBER PLATE, MODEL 1208-41FXXL, SACRAL PLATE, MODEL 1208-41FXXS ↗U.S. Food and Drug Administration · regulatory record

[23] FDA K092046 — BI-OSTETIC FOAM AND PUTTY, GENEROS FOAM AND PUTTY ↗U.S. Food and Drug Administration · regulatory record

[24] FDA K092211 — CHESAPEAKE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[25] FDA K092474 — PYRENEES CERVICAL PLATE SYSTEM, SEMI-CONSTRAINED SCREWS ↗U.S. Food and Drug Administration · regulatory record

[26] FDA K092640 — CASPIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[27] FDA K093534 — MODIFICATION TO CASPIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[28] FDA K100061 — CAYMAN SCREWS MODEL K2-12-1000-XX, K2-12-1001-XX ↗U.S. Food and Drug Administration · regulatory record

[29] FDA K100851 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[30] FDA K101084 — CASPIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[31] FDA K101302 — ALEUTIAN IBF SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[32] FDA K103169 — ALEUTTIAN ↗U.S. Food and Drug Administration · regulatory record

[33] FDA K103232 — CASPIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[34] FDA K103440 — EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[35] FDA K103797 — K2M COCR WIRE ↗U.S. Food and Drug Administration · regulatory record

[36] FDA K110843 — ALEUTIAN SPACER SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[37] FDA K110991 — MESA SPINAL SYSTEM (KEYSTONE RODS) ↗U.S. Food and Drug Administration · regulatory record

[38] FDA K111135 — PYRENEES CERVICAL PLATE SYSTEM (TRANSLATIONAL PLATES) ↗U.S. Food and Drug Administration · regulatory record

[39] FDA K111294 — SANTORINI SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[40] FDA K111439 — CHESAPEAKE (CERVICAL COMPONENTS) ↗U.S. Food and Drug Administration · regulatory record

[41] FDA K112037 — RANGE SPINAL SYSTEM (MESA AND DENALI) ↗U.S. Food and Drug Administration · regulatory record

[42] FDA K112920 — RANGE SPINAL SYSTEM (MESA AND DENALI) ↗U.S. Food and Drug Administration · regulatory record

[43] FDA K113138 — ALEUTIAN SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[44] FDA K113329 — K2M, PYRENEES CERVICAL PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[45] FDA K113654 — CASPIAN ↗U.S. Food and Drug Administration · regulatory record

[46] FDA K120031 — CHESAPEAKE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[47] FDA K120099 — RANGE SPINAL SYSTEM (MESA AND DENALI) ↗U.S. Food and Drug Administration · regulatory record

[48] FDA K120656 — EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[49] FDA K120899 — RANGE SPINAL SYSTEM, UNIT ROD ↗U.S. Food and Drug Administration · regulatory record

[50] FDA K121016 — RANGE SPINAL SYSTEM (MESA AND DENALI) ↗U.S. Food and Drug Administration · regulatory record

[51] FDA K121630 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[52] FDA K121808 — CASIAN, 3.5/4.5 CONNECTORS ↗U.S. Food and Drug Administration · regulatory record

[53] FDA K122877 — RANGE SPINAL SYSTEM, SMALL STATURE ↗U.S. Food and Drug Administration · regulatory record

[54] FDA K123412 — RANGE SPINAL SYSTEM, SMALL STRATURE COMPONENTS ↗U.S. Food and Drug Administration · regulatory record

[55] FDA K130330 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[56] FDA K130699 — ALEUTIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[57] FDA K131030 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[58] FDA K131533 — CAYMAN MI PLATE SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[59] FDA K131784 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[60] FDA K132361 — EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[61] FDA K132757 — EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[62] FDA K133288 — CASPIAN OCT SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[63] FDA K133402 — K2M MODULAR HOOKS ↗U.S. Food and Drug Administration · regulatory record

[64] FDA K133494 — CHESAPEAKE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[65] FDA K133614 — ALEUTIAN IBF SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[66] FDA K133944 — RANGE, SPINAL SYSTEM, EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[67] FDA K140529 — EVEREST SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[68] FDA K140765 — RANGE/MESA/DENALI SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[69] FDA K141147 — RANGE SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[70] FDA K141284 — CASPIAN SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[71] FDA K141873 — RANGE/MESA/DENALI SPINAL SYSTEM ↗U.S. Food and Drug Administration · regulatory record

[72] FDA K142016 — CAPRI ↗U.S. Food and Drug Administration · regulatory record

[73] FDA K142212 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[74] FDA K142360 — Everest Spinal System ↗U.S. Food and Drug Administration · regulatory record

[75] FDA K142487 — Chesapeake Stabilization System ↗U.S. Food and Drug Administration · regulatory record

[76] FDA K142558 — Caspian OCT/MESA Mini/DENALI Mini Spinal System ↗U.S. Food and Drug Administration · regulatory record

[77] FDA K143334 — Range/Denali/Mesa Spinal System ↗U.S. Food and Drug Administration · regulatory record

[78] FDA K143350 — Nile Alternative Fixation ↗U.S. Food and Drug Administration · regulatory record

[79] FDA K150325 — Range/Denali/Mesa Spinal System ↗U.S. Food and Drug Administration · regulatory record

[80] FDA K150481 — Cascadia Interbody System ↗U.S. Food and Drug Administration · regulatory record

[81] FDA K150983 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[82] FDA K151216 — Everest Spinal System ↗U.S. Food and Drug Administration · regulatory record

[83] FDA K151481 — Sahara Stabilization System ↗U.S. Food and Drug Administration · regulatory record

[84] FDA K151727 — Everest Spinal System ↗U.S. Food and Drug Administration · regulatory record

[85] FDA K152015 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[86] FDA K152281 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[87] FDA K152568 — C-VBR ↗U.S. Food and Drug Administration · regulatory record

[88] FDA K152872 — K2M Fenestrated Tap System ↗U.S. Food and Drug Administration · regulatory record

[89] FDA K153031 — RANGE/DENALI/MESA Spinal System ↗U.S. Food and Drug Administration · regulatory record

[90] FDA K153370 — Caspian OCT/MESA Mini/DENALI Mini Spinal System ↗U.S. Food and Drug Administration · regulatory record

[91] FDA K153526 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[92] FDA K160125 — Cascadia Interbody System ↗U.S. Food and Drug Administration · regulatory record

[93] FDA K160208 — NILE Alternative Fixation Spinal System ↗U.S. Food and Drug Administration · regulatory record

[94] FDA K160547 — Cascadia Interbody System ↗U.S. Food and Drug Administration · regulatory record

[95] FDA K161028 — K2M Growing Spine System ↗U.S. Food and Drug Administration · regulatory record

[96] FDA K161332 — NILE Proximal Fixation Spinal System ↗U.S. Food and Drug Administration · regulatory record

[97] FDA K161369 — EVEREST Spinal System ↗U.S. Food and Drug Administration · regulatory record

[98] FDA K162264 — Cascadia Interbody System ↗U.S. Food and Drug Administration · regulatory record

[99] FDA K162664 — Pyrenees Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[100] FDA K163364 — MOJAVE Expandable Interbody System ↗U.S. Food and Drug Administration · regulatory record

[101] FDA K170055 — CAPRI Corpectomy Cage System ↗U.S. Food and Drug Administration · regulatory record

[102] FDA K171097 — MOJAVE Expandable Interbody System ↗U.S. Food and Drug Administration · regulatory record

[103] FDA K171321 — K2M Navigation Instruments ↗U.S. Food and Drug Administration · regulatory record

[104] FDA K171444 — YUKON OCT Spinal System ↗U.S. Food and Drug Administration · regulatory record

[105] FDA K171556 — K2M Navigation Instruments ↗U.S. Food and Drug Administration · regulatory record

[106] FDA K171704 — CAPRI Corpectomy Cage System ↗U.S. Food and Drug Administration · regulatory record

[107] FDA K171832 — Range/Denali/Mesa Spinal System ↗U.S. Food and Drug Administration · regulatory record

[108] FDA K172009 — Cascadia Interbody System ↗U.S. Food and Drug Administration · regulatory record

[109] FDA K172104 — Ozark(tm) Cervical Plate System ↗U.S. Food and Drug Administration · regulatory record

[110] FDA K172941 — CASCADIA Interbody System ↗U.S. Food and Drug Administration · regulatory record

[111] FDA K173508 — Everest Spinal System ↗U.S. Food and Drug Administration · regulatory record

[112] FDA K180376 — K2M Patient Specific Rods ↗U.S. Food and Drug Administration · regulatory record

[113] FDA K180665 — SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System ↗U.S. Food and Drug Administration · regulatory record

[114] FDA K180777 — K2M Expandable Interbody System ↗U.S. Food and Drug Administration · regulatory record

[115] FDA K181119 — Range (Denali and Mesa) Spinal Systems ↗U.S. Food and Drug Administration · regulatory record

[116] FDA K181188 — EVEREST Spinal System ↗U.S. Food and Drug Administration · regulatory record

[117] FDA K181603 — EVEREST Spinal System, RANGE (MESA and DENALI) Spinal System, CASPIAN OCT (MESA Mini and DENALI Mini) Spinal System, YUKON OCT Spinal System ↗U.S. Food and Drug Administration · regulatory record

[118] FDA K181890 — Brainlab Compatible K2M Navigation Instruments ↗U.S. Food and Drug Administration · regulatory record

[119] FDA K182182 — YUKON OCT Spinal System ↗U.S. Food and Drug Administration · regulatory record

[120] FDA K182473 — PYRENEES Cervical Plate System, BLUE RIDGE Cervical Plate System, OZARK Cervical Plate System, CAYMAN Thoracolumbar and Buttress Plate Systems ↗U.S. Food and Drug Administration · regulatory record

[121] FDA K190179 — SAHARA Stabilization System ↗U.S. Food and Drug Administration · regulatory record

[122] FDA K190584 — CAYMAN LP Plate System ↗U.S. Food and Drug Administration · regulatory record

[123] FDA K192911 — Brainlab Compatible K2M Navigation Instruments ↗U.S. Food and Drug Administration · regulatory record

[124] FDA K193129 — Yukon OCT Spinal System ↗U.S. Food and Drug Administration · regulatory record

[125] FDA K193203 — MOJAVE Expandable Interbody System ↗U.S. Food and Drug Administration · regulatory record

[126] FDA K201006 — K2M Navigation Instruments ↗U.S. Food and Drug Administration · regulatory record

[127] FDA K202528 — Cannulated Power Driver Attachment ↗U.S. Food and Drug Administration · regulatory record

[128] FDA K211320 — CAPRI Corpectomy Cage System ↗U.S. Food and Drug Administration · regulatory record

[129] FDA K221490 — Tritanium C Anterior Cervical Cage, Tritanium PL Cage, Tritanium TL Curved Posterior Lumbar Cage, Tritanium X PL Expandable Posterior Lumbar Cage, Tritanium X TL Expandable Curved Posterior Lumbar Cage, Stryker Spine VLIFT Vertebral Body Replacement System, VLIFT-s Vertebral Body Replacement System, Ascential IBD PEEKc Spacer, Aero-AL Lumbar Cage System, Aero-LL Lumbar Cage System, Aero-C Cervical Cage System, AVS Aria PEEK Spacer, AVS Anchor-C Cervical Cage System, AVS Anchor-L Spacer ↗U.S. Food and Drug Administration · regulatory record

[130] FDA K242361 — OZARK Cervical Plate System; PYRENEES® Cervical Plate System; EVEREST® Spinal System; MESA® Spinal System; MESA® Small Stature Spinal System; CASPIAN® Spinal System; DENALI® Spinal System; DENALI® MI Spinal System; YUKON OCT Spinal System; Xia® 3 Spinal System; K2M Patient Specific; CASCADIA Interbody System; CAYMAN® Plate System; CAYMAN® Plate System-MI ↗U.S. Food and Drug Administration · regulatory record

[131] FDA K252873 — Q Interbody Instruments ↗U.S. Food and Drug Administration · regulatory record

[132] FDA K253545 — Vulcan Spinal System ↗U.S. Food and Drug Administration · regulatory record

[133] FDA K260546 — Q Pedicle Instruments ↗U.S. Food and Drug Administration · regulatory record

[134] FDA De Novo database — research search ↗FDA / openFDA · regulatory record

[135] FDA medical-device recall database — research search ↗FDA / openFDA · regulatory record

[136] FDA PMA database — research search ↗FDA / openFDA · regulatory record

[137] FDA recall Z-1491-2019 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[138] FDA recall Z-1492-2019 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[139] FDA recall Z-0110-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[140] FDA recall Z-0052-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[141] FDA recall Z-2008-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[142] FDA recall Z-2009-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[143] FDA recall Z-2010-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[144] FDA recall Z-2011-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[145] FDA recall Z-2012-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[146] FDA recall Z-2013-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[147] FDA recall Z-2014-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[148] FDA recall Z-2015-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[149] FDA recall Z-2016-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[150] FDA recall Z-2017-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[151] FDA recall Z-2018-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[152] FDA recall Z-2019-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[153] FDA recall Z-2020-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[154] FDA recall Z-2021-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[155] FDA recall Z-2022-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[156] FDA recall Z-2023-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[157] FDA recall Z-2024-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[158] FDA recall Z-2025-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[159] FDA recall Z-2026-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[160] FDA recall Z-2027-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[161] FDA recall Z-2028-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[162] FDA recall Z-2029-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[163] FDA recall Z-2030-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[164] FDA recall Z-2031-2020 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[165] FDA recall Z-0542-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[166] FDA recall Z-0520-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[167] FDA recall Z-0931-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[168] FDA recall Z-1410-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[169] FDA recall Z-1695-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[170] FDA recall Z-1696-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[171] FDA recall Z-1697-2021 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[172] FDA recall Z-0104-2022 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[173] FDA recall Z-0705-2022 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[174] FDA recall Z-0706-2022 — K2M, Inc ↗U.S. Food and Drug Administration · regulatory record

[175] FDA recall Z-1307-2022 — K2M, Inc. ↗U.S. Food and Drug Administration · regulatory record

[176] FDA medical-device recall database — research search ↗FDA / openFDA · regulatory record

[177] FDA UDI database — research search ↗FDA / openFDA · regulatory record

[178] Hiring source review ↗VB Spine · company website

[179] Active role: Onsite Desktop Support – IT End User Services ↗VB Spine · company website

[180] Active role: Lead End User Services Engineer ↗VB Spine · company website

[181] Active role: Sales Compensation Analyst ↗VB Spine · company website

[182] Active role: Director, FP&A ↗VB Spine · company website

[183] Active role: Strategic Sales Manager (West) ↗VB Spine · company website

[184] Active role: Product Packager ↗VB Spine · company website

[185] Active role: Associate Clinical Representative ↗VB Spine · company website

[186] Active role: Sr. Field Inventory Coordinator ↗VB Spine · company website

[187] Active role: Medical Sales Representative- 12 month FTC ↗VB Spine · company website

[188] Active role: Spine Sales Associate (Chicago, IL) ↗VB Spine · company website

[189] FDA 510(k) K253545 ↗U.S. Food and Drug Administration · regulatory database

[190] VB Spine Holdings SEC Form D: US$5 million sold ↗U.S. Securities and Exchange Commission (issuer filing) · regulatory filing

[191] VB Spine | Patient-First Spine Care Solutions ↗VB Spine · company website

[192] Current leadership and operating locations ↗VB Spine · company website

[193] Spine Surgery Products & Technologies | VB Spine ↗VB Spine · company website

[194] Vulcan first clinical cases ↗VB Spine · company website

[195] xvision spine platform transaction completed ↗VB Spine · company website

[196] Company formation and acquisition ↗VB Spine · company website