Home › Device types › MAI
Fastener, Fixation, Biodegradable, Soft Tissue
FDA product code MAI · Class 2 · Orthopedic
2,275
Registered devices
17,071
Adverse events
97
Recalls
221
510(k) clearances
Devices with this code
PANALOK ETHIBOND — DEPUY MITEK, LLCREUNITE SCREW SYSTEM — Biomet Orthopedics, LLCArthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.Fix2Lock — OSTEONIC CO.,Ltd.REUNITE SCREW SYSTEM — Biomet Orthopedics, LLCActivaScrew™ Interference — Bioretec OyGentle Threads — Biomet Orthopedics, LLCArthrex® — ARTHREX, INC.HEALIX ADVANCE BR ANCHOR w/DYNACORD — Medos International SàrlTI SCREW ES — Biomet Orthopedics, LLCREUNITE SCREW SYSTEM — Biomet Orthopedics, LLCArthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.GENESYS CrossFT, Hi-Fi — Conmed CorporationArthrex® — ARTHREX, INC.Arthrex® — ARTHREX, INC.REUNITE SCREW SYSTEM — Biomet Orthopedics, LLCMILAGRO — DEPUY MITEK, LLCArthrex® — ARTHREX, INC.LUPINE ORTHOCORD — Medos International SàrlArthrex® — ARTHREX, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-14 | ConMed Corporation | Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2025-12-17 | Aju Pharm Co., Ltd. | Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. |
| 2023-04-13 | DePuy Mitek, Inc., a Johnson & Johnson Co. | IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS Anchor Inserter may cause a fragment of the inserter tip to break off |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.