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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