Company ยท US
Synovis Life Technologies, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2013 to 2023. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 7, 2023 | K223052 | Peri-Guard and Supple Peri-Guard Synovis Life Technologies, Inc. | FTM |
| Oct 19, 2022 | K221032 | Vascu-Guard Vascular Repair Patch Synovis Life Technologies, Inc. | PSQ |
| Oct 19, 2022 | K221029 | PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch Synovis Life Technologies, Inc. | PSQ |
| Jan 16, 2015 | K143589 | GEM Flow COUPLER Device and System Synovis Life Technologies, Inc. | MVR |
| Jan 7, 2015 | K142447 | PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch Synovis Life Technologies, Inc. | DXZ |
| Nov 25, 2014 | K142461 | VASCU-GUARD Peripheral Vascular Patch Synovis Life Technologies, Inc. | DXZ |
| Sep 16, 2014 | K142309 | GEM Flow COUPLER Device and System Synovis Life Technologies, Inc. | MVR |
| Oct 22, 2013 | K132727 | GEM FLOW COUPLER DEVICE AND SYSTEM Synovis Life Technologies, Inc. | MVR |
| Apr 24, 2013 | K130896 | VASCULAR PROBE, VASCULAR PROBE ES Synovis Life Technologies, Inc. | DWP |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||