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Implantable Post-Surgical Kinematic Measurement Knee Device

FDA product code QPP · Class 2 · Orthopedic

13
Registered devices
3
Adverse events
1
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-05-02Canary Medical, Inc.Due to labeling error. Product incorrectly labeled.

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