A single-lumen surgical device intended to be percutaneously inserted into a joint to create an access port for an arthroscope/arthroscopic instrument during arthroscopy. The cannula is designed to facilitate the passage of surgical instruments while preventin
| Company | Devices | Share |
|---|---|---|
| Arthrex, Inc. | 69 | 18% |
| Biomet Orthopedics, Llc | 63 | 17% |
| T.A.G Medical Products Agricultural Cooperative Association | 50 | 13% |
| Smith & Nephew, Inc. | 36 | 10% |
| Stryker Corporation | 27 | 7% |
| Conmed Corporation | 26 | 7% |
| Medos International Sàrl | 16 | 4% |
| Medacta International Sa | 16 | 4% |
| Santa Barbara Imaging Systems, Inc. | 15 | 4% |
| Medline Industries, Inc. | 7 | 2% |
| Suzhou Endophix Co., Ltd. | 6 | 2% |
| Cannuflow, Inc. | 6 | 2% |
Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| GEA | CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY | 93 |
| NBH | Accessories, arthroscopic | 89 |
| GEA | Cannula, Surgical, General & Plastic Surgery | 79 |
| NBH | ACCESSORIES,ARTHROSCOPIC | 41 |
| NBH | Accessories, Arthroscopic | 38 |
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | 18 |
Use these as the dimensions to specify in a tender line.
376 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic access cannula, single-use", from 28 companies. The largest labeler is Arthrex, Inc. with 18% of records.
GEA (CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY), NBH (Accessories, arthroscopic), GEA (Cannula, Surgical, General & Plastic Surgery), NBH (ACCESSORIES,ARTHROSCOPIC)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.