Synovis Life Technologies, Inc.
Medical device manufacturer in St. Paul, MN.
9510(k) clearances
0PMA approvals
0recalls
Device types
510(k) clearances
| 510(k) | Device | Decision |
|---|---|---|
| K223052 | Peri-Guard and Supple Peri-GuardFTM · Traditional | 04/07/2023SE |
| K221032 | Vascu-Guard Vascular Repair PatchPSQ · Traditional | 10/19/2022SE |
| K221029 | PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair PatchPSQ · Traditional | 10/19/2022SE |
| K143589 | GEM Flow COUPLER Device and SystemMVR · Special | 01/16/2015SE |
| K142447 | PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair PatchDXZ · Traditional | 01/07/2015SE |
| K142461 | VASCU-GUARD Peripheral Vascular PatchDXZ · Traditional | 11/25/2014SE |
| K142309 | GEM Flow COUPLER Device and SystemMVR · Special | 09/16/2014SE |
| K132727 | Gem Flow Coupler Device and SystemMVR · Special | 10/22/2013SE |
| K130896 | Vascular Probe, Vascular Probe EsDWP · Traditional | 04/24/2013SE |