Kiscomedica S.A.
FDA Regulatory Profile
Kiscomedica S.A. appears in FDA public data with 1 recall, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1461-2017, Class II) was initiated on January 11, 2017. Its most recent 510(k) clearance was granted on June 30, 2008.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1461-2017 | Class II | L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage | January 11, 2017 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K080537 | L-VARLOCK | June 30, 2008 |