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Companies / Tigon Medical
Medical device company profile

Tigon Medical

Sports-medicine implants, suture systems and surgical instruments with a reusable-instrumentation focus.

Medical Device ManufacturerOrthopedics & MusculoskeletalFoot & AnkleSports Medicine & Soft Tissue RepairCommercial-stage
HeadquartersπŸ‡ΊπŸ‡ΈUnited States
Founded2017
Commercial statusCommercially availableSelected products commercially offered; availability and indications vary by product and market.
EmployeesNot confirmed
Estimated revenueNot confirmed
Official websitetigonmedical.com β†—

Company overview

Tigon Medical develops implants and instruments for sports-medicine procedures involving the shoulder and foot and ankle. The company says Jeremy Clark founded it in 2017 and that its first products received marketing clearance in 2019. Its product materials cover suture anchors, fixation systems, sutures, cannulas and instrument sets.

The GreenRepair approach emphasizes reducing disposable surgical packaging and instrumentation waste. This is a product and workflow strategy; environmental and clinical superiority claims should be evaluated against the relevant studies and comparison methods rather than assumed from the brand.

FDA decisions document multiple anchor and fixation families, including tissue anchors, all-suture anchors, Javelin devices and the FIRE system. Those decisions are distinct from individual SKUs and surgical technique names. The company website currently identifies Clark as President/Founder, which is the title used here.

[15][16][17][18]

Leadership

2 people
Jeremy ClarkPresident & Founder [15]
Zac SullivanDirector of Sales [15]

Products & regulatory status How does MedTechIndex get this information?

Summary

Tigon’s fixation portfolio has multiple 510(k) decisions, including a Button System decision K211049 absent from the earlier research. Its relationship to the currently selected FIRE/anchor configurations is kept separate. GreenRepair describes a design/commercial approach, not an FDA designation. [18][21][3][15][16][1]

No matching FDA recall event was identified in the completed company/applicant, linked-identifier and product-name searches. [12][10]

Regulatory snapshot How to read this snapshot

U.S. FDA
6
510(k) clearances
0
De Novo grants
0
PMA approvals
0
Recall events

Latest recorded source review: 2026-10-20.

Commercial portfolio snapshot

Documented commercial product families.

Bone fixation system

FIRE fixation system β†—

Fractures, Instability, and Reconstruction system listed in FDA records. [18][21]

FDA-cleared

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

Commercial development

Current product development spans soft-tissue fixation, bone fixation and reusable surgical instrumentation. GreenRepair is a commercial design philosophy, not an FDA authorization category. [15][18]

Activity & Milestones

2 events
2026-04-21 Β· Regulatory

Static Javelin anchor clearance

FDA recorded a decision for the Static Javelin and Javelin all-suture anchor line. [24]

2017 Β· Corporate

Company founded

Official company history dates foundation to 2017. [15]

24 Cited Sources

Accessed 10/20/2026

[1] FDA 510(k) database β€” research search β†—FDA / openFDA Β· regulatory record
[2] FDA K182507 β€” Tigon Medical Tissue Anchors β†—U.S. Food and Drug Administration Β· regulatory record
[3] FDA K211049 β€” Tigon Medical Button System β†—U.S. Food and Drug Administration Β· regulatory record
[4] FDA K220464 β€” Tigon Medical Gryphon Anchor Line β†—U.S. Food and Drug Administration Β· regulatory record
[6] FDA K242529 β€” Tigon Medical All-Suture Anchors (ASA) β†—U.S. Food and Drug Administration Β· regulatory record
[9] FDA De Novo database β€” research search β†—FDA / openFDA Β· regulatory record
[11] FDA PMA database β€” research search β†—FDA / openFDA Β· regulatory record
[13] FDA UDI database β€” research search β†—FDA / openFDA Β· regulatory record
[17] Instructions for use library β†—Tigon Medical Β· company website
[18] Products and current families β†—Tigon Medical Β· company website
[19] FDA 510(k) K182507 β†—U.S. Food and Drug Administration Β· regulatory database
[20] FDA 510(k) K220464 β†—U.S. Food and Drug Administration Β· regulatory database
[21] FDA 510(k) K240175 β†—U.S. Food and Drug Administration Β· regulatory database
[22] FDA 510(k) K242529 β†—U.S. Food and Drug Administration Β· regulatory database
[23] FDA 510(k) K252596 β†—U.S. Food and Drug Administration Β· regulatory database
[24] FDA 510(k) K260921 β†—U.S. Food and Drug Administration Β· regulatory database
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