CORIN MEDICAL, LTD.
FDA Regulatory Profile
CORIN MEDICAL, LTD. appears in FDA public data with 1 recall, 1 510(k) clearance, 6 FDA inspections, and 1 compliance action on record. Its most recent recall (Z-2069-2025, Class II) was initiated on May 23, 2025. Its most recent 510(k) clearance was granted on March 8, 2013.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 6
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-2069-2025 | Class II | Apex Knee System. Model Numbers: KC-50090, KC-50097, KC-50110, KC-50117, KC-50130, KC-50135, KC-5013 | May 23, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K130128 | TRINITY ACETABULAR SYSTEM | March 8, 2013 |