Synovis Micro Companies Alliance, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Synovis Micro Companies Alliance, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GEM Biover Microvascular Clamps, GEM FLOW COUPLER Monitor (GEM1020M-2)
4
Total
4
Cleared
0
Denied
Synovis Micro Companies Alliance, Inc. has 4 FDA 510(k) cleared medical devices. Based in Birmingham, US.
Last cleared in 2022. Active since 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Synovis Micro Companies Alliance, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Synovis Micro Companies Alliance, Inc.
4 devices
Cleared
Sep 14, 2022
GEM Biover Microvascular Clamps
Cardiovascular
82d
Cleared
Apr 20, 2022
GEM FLOW COUPLER Monitor (GEM1020M-2)
General & Plastic Surgery
121d
Cleared
Feb 01, 2010
GEM FLOW COUPLER DEVICE AND SYSTEM
General & Plastic Surgery
102d
Cleared
Apr 16, 2004
MICROVASCULAR ANASTOMOTIC DEVICE
General & Plastic Surgery
81d