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FDA 510(k) Applications Submitted by Synovis Life Technologies, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K143589
12/18/2014
GEM Flow COUPLER Device and System
Synovis Life Technologies, Inc.
K221029
04/07/2022
PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch
Synovis Life Technologies, Inc.
K223052
09/29/2022
Peri-Guard and Supple Peri-Guard
Synovis Life Technologies, Inc.
K221032
04/07/2022
Vascu-Guard Vascular Repair Patch
Synovis Life Technologies, Inc.
K130896
04/01/2013
VASCULAR PROBE, VASCULAR PROBE ES
SYNOVIS LIFE TECHNOLOGIES, INC.
K142309
08/19/2014
GEM Flow COUPLER Device and System
Synovis Life Technologies, Inc.
K132727
09/03/2013
GEM FLOW COUPLER DEVICE AND SYSTEM
SYNOVIS LIFE TECHNOLOGIES, INC.
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