# Synovis Life Technologies, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 9 (2013–2023): 9 510(k) clearances
- Product codes: MVR (3), DXZ (2), PSQ (2), DWP (1), FTM (1)
- Predicates its devices cite: 13 (4 its own); citations of its devices by later devices: 6 (4 its own)
- Recalls linked to its devices: 15 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bio-Vascular, Inc.: 7 (https://510kreport.com/company/bio-vascular)
- Synovis Micro Companies Alliance, Inc.: 2 (https://510kreport.com/company/synovis-micro-companies-alliance)

## Firms that cite its devices most
- Synovis Micro Companies Alliance, Inc.: 1 (https://510kreport.com/company/synovis-micro-companies-alliance)
- Baxter/ Synovis Micro Companies Alliance, Inc.: 1 (https://510kreport.com/company/baxter-synovis-micro-companies-alliance)

## Its most-cited devices
- K143589: GEM Flow COUPLER Device and System (2015), cited by 2
- K142461: VASCU-GUARD Peripheral Vascular Patch (2014), cited by 1
- K132727: Gem Flow Coupler Device and System (2013), cited by 1
- K142309: GEM Flow COUPLER Device and System (2014), cited by 1
- K142447: PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch (2015), cited by 1

## Recent decisions
- K223052: Peri-Guard and Supple Peri-Guard (Apr 7, 2023)
- K221029: PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch (Oct 19, 2022)
- K221032: Vascu-Guard Vascular Repair Patch (Oct 19, 2022)
- K143589: GEM Flow COUPLER Device and System (Jan 16, 2015)
- K142447: PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch (Jan 7, 2015)
- K142461: VASCU-GUARD Peripheral Vascular Patch (Nov 25, 2014)
- K142309: GEM Flow COUPLER Device and System (Sep 16, 2014)
- K132727: Gem Flow Coupler Device and System (Oct 22, 2013)

Source page: https://510kreport.com/company/synovis-life-technologies