Kico Knee Innovation Company
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Mode recall (Z-2957-2026) | Kico Knee Innovation Company | 2026-08-14 |
| Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following compone recall (Z-2292-2026) | Kico Knee Innovation Company | 2026-06-02 |
| Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following compone recall (Z-2293-2026) | Kico Knee Innovation Company | 2026-06-02 |
| Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surg recall (Z-0145-2026) | Kico Knee Innovation Company | 2025-10-14 |
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Every clearance here is in the API, with alerts when new ones post.