FDA Device Intelligence
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Instrument, Compression

FDA product code HWN · Class 1 · Orthopedic

742
Registered devices
822
Adverse events
9
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer Inc.The firm determined that the recalled instruments were manufactured using the wrong grade of material. As manufactured, the instruments are more brittle, incre
2010-02-16Zimmer 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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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.