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Kico Knee Innovation Company

4 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Mode recall (Z-2957-2026)Kico Knee Innovation Company2026-08-14
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following compone recall (Z-2292-2026)Kico Knee Innovation Company2026-06-02
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following compone recall (Z-2293-2026)Kico Knee Innovation Company2026-06-02
Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surg recall (Z-0145-2026)Kico Knee Innovation Company2025-10-14

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