Synovis Life Technologies, Inc.
Synovis Life Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2023.
Top product codes for Synovis Life Technologies, Inc.
Recent clearances by Synovis Life Technologies, Inc.
- K223052 — Peri-Guard and Supple Peri-Guard
- K221029 — PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch
- K221032 — Vascu-Guard Vascular Repair Patch
- K143589 — GEM Flow COUPLER Device and System
- K142447 — PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch
- K142461 — VASCU-GUARD Peripheral Vascular Patch
- K142309 — GEM Flow COUPLER Device and System
- K132727 — GEM FLOW COUPLER DEVICE AND SYSTEM
- K130896 — VASCULAR PROBE, VASCULAR PROBE ES
Data sourced from openFDA. This site is unofficial and independent of the FDA.