Synovis Life Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synovis Life Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Peri-Guard and Supple Peri-Guard, PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch, Vascu-Guard Vascular Repair Patch
9
Total
9
Cleared
0
Denied
Synovis Life Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Last cleared in 2023. Active since 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Synovis Life Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synovis Life Technologies, Inc.
9 devices
Cleared
Apr 07, 2023
Peri-Guard and Supple Peri-Guard
General & Plastic Surgery
190d
Cleared
Oct 19, 2022
PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch
Cardiovascular
195d
Cleared
Oct 19, 2022
Vascu-Guard Vascular Repair Patch
Cardiovascular
195d
Cleared
Jan 16, 2015
GEM Flow COUPLER Device and System
General & Plastic Surgery
29d
Cleared
Jan 07, 2015
PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch
Cardiovascular
127d
Cleared
Nov 25, 2014
VASCU-GUARD Peripheral Vascular Patch
Cardiovascular
84d
Cleared
Sep 16, 2014
GEM Flow COUPLER Device and System
General & Plastic Surgery
28d
Cleared
Oct 22, 2013
GEM FLOW COUPLER DEVICE AND SYSTEM
General & Plastic Surgery
49d
Cleared
Apr 24, 2013
VASCULAR PROBE, VASCULAR PROBE ES
Cardiovascular
23d