Kico Knee Innovation Company
Kico Knee Innovation Company appears in FDA public data with 3 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2292-2026, Class II) was initiated on April 23, 2026.
Summary
- Total Recalls
- 3
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2292-2026 | Class II | Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10 | April 23, 2026 |
| Z-2293-2026 | Class II | Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10 | April 23, 2026 |
| Z-0145-2026 | Class II | Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Pla | September 19, 2025 |