Home › Device types › KWD
Prosthesis, Toe, Hemi-, Phalangeal
FDA product code KWD · Class 2 · Orthopedic
486
Registered devices
294
Adverse events
13
Recalls
46
510(k) clearances
Devices with this code
Trigon — NVision Biomedical Technologies, Inc.BioMotion Cannulated 1st MPJ Hemi System — Smith & Nephew, Inc.LMH — WRIGHT MEDICAL TECHNOLOGY, INC.VOLANS — HNM TOTAL RECON LLCOsteoMed — OSTEOMED LLCTOE JOINT COBALT CHROME NPC M/L 21.5MM — BIOPRO, INC.Cannulated 1st MPJ Hemi Implant — VILEX LLCAccu-Joint — Accufix Surgical, Inc.TOE JOINT COBALT CHROME NPC SM 17MM — BIOPRO, INC.NAOS — HNM TOTAL RECON LLCBaseCap — ARTHROSURFACE INCORPORATEDSWANSON — WRIGHT MEDICAL TECHNOLOGY, INC.HemiCAPDF® — ARTHROSURFACE INCORPORATEDAccu-Joint — Accufix Surgical, Inc.VOLANS — HNM TOTAL RECON LLCAccu-Joint — Accufix Surgical, Inc.TOE NON POROUS COATED SMALL 17mm — BIOPRO, INC.HemiCAPDF® — ARTHROSURFACE INCORPORATEDCannulated 1st MPJ Hemi Implant — VILEX LLCMovement Great Toe System — Smith & Nephew, Inc.TOE JOINT NPC 8.00MM W/HOLE — BIOPRO, INC.ORTHOSPHERE — WRIGHT MEDICAL TECHNOLOGY, INC.Movement® — Ascension Orthopedics, Inc.TOE POROUS COATED SMALL 17mm — BIOPRO, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
| 2022-02-01 | BioPro, Inc. | There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) |
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