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Companies / Responsive Arthroscopy
Medical device company profile

Responsive Arthroscopy

Minneapolis-based medical device company offering suture anchors, interference screws and fixation systems for sports medicine and soft-tissue repair.

Medical Device ManufacturerOrthopedics & MusculoskeletalSports Medicine & Soft Tissue RepairCommercial-stage
HeadquartersπŸ‡ΊπŸ‡ΈMinneapolis, Minnesota, United States
FoundedNot confirmed
Commercial statusCommercially availableSelected implants and instruments are commercially advertised; model availability and distribution arrangements should be confirmed with the manufacturer.
EmployeesNot confirmed
Estimated revenueNot confirmed
Official websiteresponsivesports.com β†—

Company overview

Responsive Arthroscopy develops and markets implants and instruments for orthopedic sports medicine. Its published portfolio covers procedures involving the shoulder, knee, hip, foot and ankle, including soft-tissue fixation, ligament reconstruction and syndesmosis repair.

The company’s FDA history includes interference-screw, suture-anchor and Thunderbolt fixation systems, with records under both Responsive Arthroscopy, LLC and Responsive Arthroscopy, Inc. Individual authorizations and current commercial availability are distinguished in the product and regulatory section.

Johnson & Johnson MedTech announced an exclusive U.S. commercial distribution agreement with Responsive Arthroscopy on November 14, 2024, describing a focus on sports soft-tissue repair solutions. The announcement does not specify every covered product or establish the current terms of the agreement.

[2][3][29]

Leadership

2 people
Douglas (Doug) KohrsManaging Director, President & Chief Executive Officer [30]
Gretchen HinchleyExecutive Vice President of Operations [25]

Products & regulatory status How does MedTechIndex get this information?

Summary

Responsive Arthroscopy’s reviewed FDA history contains 13 510(k) clearances under its LLC and Inc. names. Eight decisions are mapped to the selected commercially advertised screw, suture-anchor, wedge-anchor and Thunderbolt families shown below. The remaining five cover Mustang, Stealth/Mini Stealth, Shadow, Osprey and Mini Superhawk; their current commercial availability and exact mapping to the advertised portfolio were not established, so they are excluded from the snapshot totals. [13][14][15][16][17][18][19][20][21][22][23][24][25]

The latest matched decision is K261632 for Thunderbolt, dated July 20, 2026. Clearances apply to the configurations and indications in each FDA document; an earlier product photograph does not establish availability of every subsequently cleared configuration. No matching De Novo grants, original PMAs or FDA recall events were identified within the company, product-name and linked-identifier searches performed. [25][27][26][28]

Regulatory snapshot How to read this snapshot

U.S. FDA
8
510(k) clearances
0
De Novo grants
0
PMA approvals
0
Recall events

Latest recorded source review: 2026-10-22.

Commercial portfolio snapshot

Documented commercial product families.

Spirit PEEK interference screws
Image: Responsive Arthroscopy
Interference screws

Spirit Interference Screw System β†—

PEEK and titanium interference screws for tissue fixation in ligament reconstruction. The image shows the PEEK configuration. [6][8][13][18]

FDA-cleared

Commercially advertised by the manufacturer; exact models and market availability should be confirmed.

Valor knotless push-in anchors and inserters
Image: Responsive Arthroscopy
Suture anchors

PEEK Suture Anchor Systems β†—

Selected PEEK soft-tissue fixation systems presented on the company’s shoulder page include Valor, Hornet, Super Hornet, Falcon and Lightning. The image shows Valor anchors and inserters. [7][10][14][17]

FDA-cleared

Commercially advertised by the manufacturer; exact models and market availability should be confirmed.

Nighthawk shoulder labrum anchor and instrument tray
Image: Responsive Arthroscopy
Knotless suture anchors

Nighthawk Wedge Push-In Suture Anchors β†—

Knotless PEEK wedge-anchor systems for soft-tissue fixation, with shoulder and hip configurations documented by the manufacturer. [7][5][9][15][16]

FDA-cleared

Commercially advertised by the manufacturer; exact models and market availability should be confirmed.

Thunderbolt fixation implants and instrument tray
Image: Responsive Arthroscopy
Suture-button fixation

Thunderbolt System β†—

Suture-button fixation system offered for syndesmosis repair, with an optional two-hole plate. FDA records also describe additional labeled soft-tissue fixation applications. The image shows the manufacturer’s published earlier configuration. [4][11][19][25]

FDA-cleared

Commercially advertised by the manufacturer; exact models and market availability should be confirmed.

Superhawk lateral ankle stabilization anchors and instruments
Image: Responsive Arthroscopy
Suture-anchor stabilization

Superhawk Lateral Ankle Stabilization System β†—

Adjustable suture-anchor system advertised for lateral ankle stabilization and Brostrom repair. This is the manufacturer’s Superhawk system, distinct from the separately cleared Mini Superhawk. [4][12]

Marketed Β· authorization mapping not established

Commercially advertised by the manufacturer; exact models and market availability should be confirmed.

Known Distribution Partners

1 partner

Publicly documented relationships; coverage may be incomplete.

PartnerTerritory / scopeProducts
Johnson & Johnson MedTech [29]United States Β· agreement announced November 2024Sports soft-tissue repair solutions; exact covered product families not specified

Sources checked October 22, 2026.

Activity & Milestones

2 events
2026-07-20 Β· Regulatory

Thunderbolt FDA clearance

FDA issued a substantially equivalent decision for the Thunderbolt System under K261632. Clearance does not establish launch timing for every cleared configuration. [25]

2024-11-14 Β· Commercial

U.S. distribution agreement announced with J&J MedTech

Johnson & Johnson MedTech announced an exclusive U.S. commercial distribution agreement for sports soft-tissue repair solutions. Exact product scope and continuing contractual terms are not independently confirmed. [29]

30 Cited Sources

Accessed 10/22/2026

[1] ClinicalTrials.gov β€” exact company research search β†—ClinicalTrials.gov Β· clinical trial registry
[2] Company website and contact details β†—Responsive Arthroscopy Β· company website
[3] Company overview and Minneapolis address β†—Responsive Arthroscopy Β· company website
[4] Foot and ankle product portfolio β†—Responsive Arthroscopy Β· company website
[5] Hip product portfolio β†—Responsive Arthroscopy Β· company website
[6] Knee product portfolio β†—Responsive Arthroscopy Β· company website
[7] Shoulder product portfolio β†—Responsive Arthroscopy Β· company website
[13] FDA K180573 β€” Responsive Arthroscopy Interference Screw System β†—FDA Β· regulatory database Β· Published 2018-11-23
[14] FDA K180951 β€” Responsive Arthroscopy Suture Anchor System β†—FDA Β· regulatory database Β· Published 2019-01-03
[17] FDA K202153 β€” Responsive Arthroscopy Suture Anchor System β†—FDA Β· regulatory database Β· Published 2020-09-09
[18] FDA K202569 β€” Responsive Arthroscopy Interference Screw System β†—FDA Β· regulatory database Β· Published 2020-09-23
[19] FDA K203121 β€” Responsive Arthroscopy Thunderbolt System β†—FDA Β· regulatory database Β· Published 2021-04-27
[22] FDA K233258 β€” Shadow Knotless All-Suture Anchors β†—FDA Β· regulatory database Β· Published 2023-10-23
[23] FDA K243726 β€” Osprey Suture Anchor β†—FDA Β· regulatory database Β· Published 2025-01-30
[24] FDA K253010 β€” Mini Superhawk Suture Anchor System β†—FDA Β· regulatory database Β· Published 2025-10-14
[25] FDA K261632 β€” Thunderbolt System β†—FDA Β· regulatory database Β· Published 2026-07-20
[29] J&J MedTech announces U.S. distribution agreement β†—Johnson & Johnson Β· press release Β· Published 2024-11-14
Company research

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