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Knife, Orthopedic

FDA product code HTS · Class 1 · Orthopedic

315
Registered devices
12
Adverse events
3
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-09-30Beaver Visitec International, Inc.Incorrect configuration of the blades in the package. The blades curve to the right instead of curving to the left. If used may cause cause unintended tissue da
2009-11-11Stryker Howmedica Osteonics Corp.Disposable Patella Cutters - 30 mm (catalog number 8000-0030, lot V31257001) were packaged and labeled as 33 mm Disposable Patella Cutters (catalog number 8000-
2009-06-12Becton Dickinson and CompanyMislabeled: Arthro-Lok Pointed Tip 4mm Blade curving right instead of left.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.