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FDA product code HWT · Class 1 · 1,654 devices · 18,687 reports · 70 devices named in recalls
- T-PAL 03.812.515Synthes GmbH · TEMPLATE2 reports
- NA 03.841.009Synthes GmbH · TEMPLATE2 reports
- SYNFIX Evolution 03.835.222Synthes GmbH · TEMPLATE2 reports
- NA 201-02-35Exactech, Inc. · TEMPLATE2 reports
- NA 201-02-38Exactech, Inc. · TEMPLATE2 reports
- Equinoxe 321-14-00Exactech, Inc. · TEMPLATE2 reports
- NA 329.607Synthes GmbH · TEMPLATE2 reports
- NA 329.64Synthes GmbH · TEMPLATE2 reports
- MatrixMANDIBLE 03.503.911Synthes GmbH · TEMPLATE2 reports
- NA 329.524Synthes GmbH · TEMPLATE2 reports
- ENDOSKELETON® TA 2112-9314Medtronic Sofamor Danek, Inc. · TEMPLATE1 report
- PRO-SPEC CALC-CUBOID TRIAL 8MMCrossroads Extremity Systems · Template1 report
- SWANSON 24370001Wright Medical Technology, Inc. · TEMPLATE1 report
- SWANSON 24370006Wright Medical Technology, Inc. · TEMPLATE1 report
- Tornier Perform MWM011Tornier, Inc. · TEMPLATE1 report
- Tornier Perform MWP4390Tornier, Inc. · TEMPLATE1 report
- Tornier Perform MWP2420Tornier, Inc. · TEMPLATE1 report
- Tornier Perform MWP2360Tornier, Inc. · TEMPLATE1 report
- Tornier HRS ARS1023303Tornier, Inc. · TEMPLATE1 report
- Tornier HRS ARS1023304Tornier, Inc. · TEMPLATE1 report
- Tornier HRS ARS1023306Tornier, Inc. · TEMPLATE1 report
- Tornier HRS ARS1023601Tornier, Inc. · TEMPLATE1 report
- Tornier HRS ARS1023603Tornier, Inc. · TEMPLATE1 report
- Tornier Perform Humeral System ARS1023803Tornier, Inc. · TEMPLATE1 report
- VANGUARD 32-487276Biomet Orthopedics, LLC · TEMPLATE1 report
- MAX-TI CAGE TRIAL 31-124220Biomet Orthopedics, LLC · TEMPLATE1 report
- ZUK 00584102108Smith & Nephew, Inc. · TEMPLATE1 report
- ZUK 00584102209Smith & Nephew, Inc. · TEMPLATE1 report
- ZUK 00584102210Smith & Nephew, Inc. · TEMPLATE1 report
- ZUK 00584102411Smith & Nephew, Inc. · TEMPLATE1 report
- ZUK 00584102510Smith & Nephew, Inc. · TEMPLATE1 report
- ZUK 00584102609Smith & Nephew, Inc. · TEMPLATE1 report
- Harmony 74033813Smith & Nephew, Inc. · TEMPLATE1 report
- JII E0015575-2Smith & Nephew, Inc. · TEMPLATE1 report
- LEGION 71434609Smith & Nephew, Inc. · TEMPLATE1 report
- LEGION 71434627Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY II 74033835Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY II 74033841Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY II 74033844Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY II 74033855Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY 74031253Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY 74031254Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY 74031256Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY 74031264Smith & Nephew, Inc. · TEMPLATE1 report
- JOURNEY 74031265Smith & Nephew, Inc. · TEMPLATE1 report
- LEGION 71433107Smith & Nephew, Inc. · TEMPLATE1 report
- AETOS Shoulder System TRL-0990-841-42ARSmith & Nephew, Inc. · TEMPLATE1 report
- Salto Talaris Total Ankle Prosthesis MJV501TSmith & Nephew, Inc. · TEMPLATE1 report
- Titan Modular Shoulder System 2.5 SZR-0926-030-010Smith & Nephew, Inc. · TEMPLATE1 report
- Titan Modular Shoulder System 2.5 SZR-0926-030-023Smith & Nephew, Inc. · TEMPLATE1 report
- Titan Reverse Shoulder System DTL-0960-08STDSmith & Nephew, Inc. · TEMPLATE1 report
- Vanguard® Premier™ Knee Instruments 32-487276Biomet Orthopedics, LLC · TEMPLATE1 report
- Arthrex® AR-601-FTLEArthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-601-TBC9Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-601-TBF8Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-601-TBP4Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-9238Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-603-79Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-603-A109Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-603-A208Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-603-A309Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-603-A908Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-623-T111Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-623-T112Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-623-T408Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-623-T509Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-623-T608Arthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-9510-05MArthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-13070M-P-TArthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-9236-03AG-15RArthrex, Inc. · TEMPLATE1 report
- Arthrex® AR-9236-03AG-15LArthrex, Inc. · TEMPLATE1 report
- MultiPolar® 5003-50-28Zimmer, Inc. · TEMPLATE1 report
- VerSys® 7895-32-02Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5881-50-14Zimmer, Inc. · TEMPLATE1 report
- NexGen® Legacy® 5961-30-10Zimmer, Inc. · TEMPLATE1 report
- NexGen® Legacy® 5961-40-12Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5971-30-10Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5981-37-01Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5981-37-02Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5981-57-01Zimmer, Inc. · TEMPLATE1 report
- NexGen® 5981-57-02Zimmer, Inc. · TEMPLATE1 report
- NexGen® Legacy® 5995-40-10Zimmer, Inc. · TEMPLATE1 report
- NexGen® Legacy® 5997-14-01Zimmer, Inc. · TEMPLATE1 report
- INFINITY 33622206Wright Medical Technology, Inc. · TEMPLATE1 report
- GRAFTMASTER 014414Smith & Nephew, Inc. · TEMPLATE1 report
- NA 7207502Smith & Nephew, Inc. · TEMPLATE1 report
- GRAFTMASTER 72202316Smith & Nephew, Inc. · TEMPLATE1 report
- NOVAE GE007-51Soc Etudes Recherches Fabrication · Template1 report
- NOVAE GE007-55Soc Etudes Recherches Fabrication · Template1 report
- NOVAE IE006 49/28Soc Etudes Recherches Fabrication · Template1 report
- AESCULAP NF770RAesculap AG · TEMPLATE1 report
- AESCULAP NF771RAesculap AG · TEMPLATE1 report
- ENDURO NP451RAesculap AG · TEMPLATE1 report
- VEGA SYSTEM PS NS824RAesculap AG · TEMPLATE1 report
- VARIAX 703832Stryker GmbH · Template1 report
- VARIAX 703836Stryker GmbH · Template1 report
- VARIAX 703841Stryker GmbH · Template1 report
- VARIAX 703843Stryker GmbH · Template1 report
- VARIAX 703852Stryker GmbH · Template1 report
- VARIAX 703856Stryker GmbH · Template1 report