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Synovis Life Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K223052	Peri-Guard and Supple Peri-Guard	FTM	2023-04-07	View
510(k)	K221032	Vascu-Guard Vascular Repair Patch	PSQ	2022-10-19	View
510(k)	K221029	PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch	PSQ	2022-10-19	View
510(k)	K132727	GEM FLOW COUPLER DEVICE AND SYSTEM	MVR	2013-10-22	View
510(k)	K130896	VASCULAR PROBE, VASCULAR PROBE ES	DWP	2013-04-24	View

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