Is this your brand? Sign in to claim ownership.
Sign in to claim this brandArthrex, Inc.
United States·US-MF-000019271
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 1370 Creekside Blvd, Naples, United States
- Website
- www.arthrex.com/
- —
- —
- [email protected]
- Phone
- +1 800 934-4404
- PRRC Contact
- Amanda Webb
- EUDAMED SRN
- US-MF-000019271
- FDA FEI Number
- 1220246
- DUNS Number
- 131747628
Catalogue (17149)
Page 1 of 343| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Arthrex Bioabsorbable PushLock Suture Anchors | K253931 | FDA 510(k) | Class II | Active |
| Arthrex® | AR-8916CX24-08 | FDA UDI | Class II | Active |
| Arthrex® | AR-9502F-36CPC | FDA UDI | Class II | Active |
| Arthrex® | AR-8500TD | FDA UDI | Class I | Active |
| Arthrex® | AR-1688C-34S | FDA UDI | Class I | Active |
| Arthrex® | AR-8967-65FT | FDA UDI | Class II | Active |
| Arthrex® | AR-1365NS-40 | FDA UDI | Class II | Active |
| Arthrex® | AR-1204F-115 | FDA UDI | Class I | Active |
| Arthrex® | AR-9094ES-12-4230L | FDA UDI | Class II | Active |
| Arthrex® | AR-12600SRF | FDA UDI | Class I | Active |
| Arthrex® | AR-8933HVCL-42S | FDA UDI | Class II | Active |
| Arthrex® | ABS-10020 | FDA UDI | Class I | Active |
| Arthrex® | AR-13307 | FDA UDI | Class I | Active |
| Arthrex® | AR-18800-37 | FDA UDI | Class I | Active |
| Arthrex® | AR-8916VWL-07 | FDA UDI | Class II | Active |
| Arthrex® | AR-600-352S | FDA UDI | Class I | Active |
| Arthrex® | AR-501-TTLA | FDA UDI | Class II | Active |
| Arthrex® | AR-1980-05S | FDA UDI | Class I | Active |
| Arthrex® | AR-12550 | FDA UDI | Class I | Active |
| Arthrex® | AR-1382T | FDA UDI | Class II | Active |
| Arthrex® | AR-8840-24S | FDA UDI | Class II | Active |
| Arthrex® | AR-4020C-07 | FDA UDI | Class II | Active |
| Arthrex® | AR-8827-30S | FDA UDI | Class II | Active |
| Arthrex® | AR-8717-0907 | FDA UDI | Class II | Active |
| Arthrex® | AR-7274T-1 | FDA UDI | Class II | Active |
| Arthrex® | AR-S3350-6315-130 | FDA UDI | Class II | Active |
| Arthrex® | AR-9093-50-046 | FDA UDI | Class II | Active |
| Arthrex® | AR-9401-18 | FDA UDI | Class I | Active |
| Arthrex® | AR-8719MXDS-2520 | FDA UDI | Class II | Active |
| Arthrex® | AR-9094ES-14-3930L | FDA UDI | Class II | Active |
| Sonoma Orthopedic Products, Inc | 2.7mm x 24mm MINI-CRX Self-Tapping, Bone Screw, Sterile | FDA UDI | Class II | Unknown |
| Arthrex® | AR-3610CTCS-2 | FDA UDI | Class I | Active |
| Sonoma Orthopedic Products, Inc | FST-32100-S | FDA UDI | Class II | Unknown |
| Arthrex® | AR-8933V-46 | FDA UDI | Class II | Active |
| Arthrex® | AR-9581-2835-2 | FDA UDI | Class II | Active |
| Arthrex® | AR-7650-20-R | FDA UDI | Class I | Active |
| Arthrex® | AR-9098-10-405 | FDA UDI | Class II | Active |
| Arthrex® | AR-9231-01AG-25R | FDA UDI | Class I | Active |
| Arthrex® | AR-9095-44S | FDA UDI | Class I | Active |
| Arthrex® | AR-613-38 | FDA UDI | Class I | Active |
| Arthrex® | AR-8840-60S | FDA UDI | Class II | Active |
| Arthrex® | AR-516-10R | FDA UDI | Class II | Active |
| Arthrex® | AR-513-BG12 | FDA UDI | Class II | Active |
| Arthrex® | AR-8954ML-S | FDA UDI | Class II | Active |
| Arthrex® | AR-1510H | FDA UDI | Class I | Active |
| Arthrex® | AR-1998T-25 | FDA UDI | Class I | Active |
| Arthrex® | AR-8670C | FDA UDI | Class I | Active |
| Arthrex® | AR-9674-10 | FDA UDI | Class I | Active |
| Arthrex® | AR-611-SB21 | FDA UDI | Class I | Active |
| Arthrex® | AR-9564-2839-LAT | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Arthrex GmbH Munich Bavaria · DE FEI 3002579136