# Arthex, Inc.

- Location (FDA's records): Naples, FL
- FDA decisions: 3 (2015–2023): 3 510(k) clearances
- Product codes: GCJ (1), PLF (1), MBI (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 4 (https://510kreport.com/company/arthrex)
- Novadaq Technologies Ulc. (Now A Part of Stryker): 1 (https://510kreport.com/company/novadaq-technologies-ulc-now-a-part-of-stryker)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Firms that cite its devices most
- Nvision Biomedical Technologies, Inc.: 2 (https://510kreport.com/company/nvision-biomedical-technologies)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Ames Medical Prosthetic Solutions, S.A.U.: 1 (https://510kreport.com/company/ames-medical-prosthetic-solutions-sau)

## Its most-cited devices
- K151256: Arthrex BioSync® Bone Wedge (2015), cited by 3
- K223759: Arthrex SynergyID Endoscopic Imaging System (2023), cited by 1

## Recent decisions
- K223759: Arthrex SynergyID Endoscopic Imaging System (Feb 24, 2023)
- K172612: FiberTak DX (Sep 28, 2017)
- K151256: Arthrex BioSync® Bone Wedge (Aug 12, 2015)

Source page: https://510kreport.com/company/arthex