Synovis Life Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223052 | Peri-Guard and Supple Peri-Guard | April 7, 2023 |
| K221032 | Vascu-Guard Vascular Repair Patch | October 19, 2022 |
| K221029 | PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch | October 19, 2022 |
| K143589 | GEM Flow COUPLER Device and System | January 16, 2015 |
| K142447 | PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch | January 7, 2015 |
| K142461 | VASCU-GUARD Peripheral Vascular Patch | November 25, 2014 |
| K142309 | GEM Flow COUPLER Device and System | September 16, 2014 |
| K132727 | GEM FLOW COUPLER DEVICE AND SYSTEM | October 22, 2013 |
| K130896 | VASCULAR PROBE, VASCULAR PROBE ES | April 24, 2013 |