# Tigon Medical

- Location (FDA's records): Millersville, MD
- FDA decisions: 7 (2019–2026): 7 510(k) clearances
- Product codes: MBI (6), HWC (1)
- 510(k) review time since 2016: median 118 days, against 63 for FDA's reviews in the same codes and years (1 of 7 faster)
- Predicates its devices cite: 13 (6 its own); citations of its devices by later devices: 6 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 3 (https://510kreport.com/company/arthrex)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Cayenne Medical, Inc.: 1 (https://510kreport.com/company/cayenne-medical)
- T.A.G. Medical Products Corporation, Ltd.: 1 (https://510kreport.com/company/tag-medical-products)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)

## Its most-cited devices
- K182507: Tigon Medical Tissue Anchors (2019), cited by 2
- K242529: Tigon Medical All-Suture Anchors (ASA) (2024), cited by 2
- K252596: Tigon Medical Knotless and Dual Javelin All-Suture Anchors (2025), cited by 1
- K220464: Tigon Medical Gryphon Anchor Line (2023), cited by 1

## Recent decisions
- K260921: Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor Line (Apr 21, 2026)
- K252596: Tigon Medical Knotless and Dual Javelin All-Suture Anchors (Dec 4, 2025)
- K242529: Tigon Medical All-Suture Anchors (ASA) (Dec 20, 2024)
- K240175: Tigon Medical Fractures, Instability, and Reconstruction (FIRE) (Oct 29, 2024)
- K220464: Tigon Medical Gryphon Anchor Line (Mar 22, 2023)
- K211049: Tigon Medical Button System (Aug 4, 2021)
- K182507: Tigon Medical Tissue Anchors (Jan 21, 2019)

Source page: https://510kreport.com/company/tigon-medical