Home › Device types › HWN
Instrument, Compression
FDA product code HWN · Class 1 · Orthopedic
753
Registered devices
852
Adverse events
9
Recalls
4
510(k) clearances
Devices with this code
NA — Synthes GmbHGauthier Biomedical — GAUTHIER BIOMEDICAL, INC.TrabecuLink Femoral and Tibial Cone - Instruments — WALDEMAR LINK GmbH & Co. KGPrecice® Fast Distractor Max — NUVASIVE SPECIALIZED ORTHOPEDICS, INC.Medtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.Metalogix Revolution — FUSION ORTHOPEDICS, LLCN/A — MEDTRONIC SOFAMOR DANEK, INC.N/A — Zimmer, Inc.LINK Instruments - Rasps, compressors and broaches — WALDEMAR LINK GmbH & Co. KGMalibu — Seaspine Orthopedics CorporationIMPLANT & INSTRUMENT STERILIZATION TRAY — BIOPRO, INC.Cosmolock — Kalitec Direct LLCTrabecuLink Femoral and Tibial Cone - Instruments — WALDEMAR LINK GmbH & Co. KGPHOENIX SFS — Orthofix US LLCAlpine XC Adjustable Fusion System — Highridge Medical, LLCTornier Flex — TORNIERVirage OCT Spinal Fixation System — Highridge Medical, LLCNewPort — Seaspine Orthopedics CorporationANAX 5.5™ Spinal System — CG MedTech Co.,Ltd.Inertia® MIS Pedicle Screw System — NEXXT SPINE, LLCMedtronic Reusable Instruments — MEDTRONIC SOFAMOR DANEK, INC.CosmoLock Pedicle Screw System — Kalitec Direct LLCN/A — MEDTRONIC SOFAMOR DANEK, INC.CosmoLock Pedicle Screw System — Kalitec Direct LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
| 2010-02-16 | Zimmer Inc. | The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre |
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