# Arthrex Arthroscopy Instruments, Inc.

- Location (FDA's records): Norwalk, CT
- FDA decisions: 2 (1988–1988): 2 510(k) clearances
- Product codes: HRX (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K881792: Cannula Model AR-6551 (Jul 7, 1988)
- K880295: Cannula Model AR-6001 (Jun 29, 1988)

Source page: https://510kreport.com/company/arthrex-arthroscopy-instruments