Synovis Life Technologies, Inc. FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Peri-Guard and Supple Peri-Guard510(k)Apr 7, 2023General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Apr 7, 2023
Vascu-Guard Vascular Repair Patch510(k)Oct 19, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Oct 19, 2022
PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair Patch510(k)Oct 19, 2022Cardiovascular	Cardiovascular	510(k)Substantially Equivalent (Traditional)	Oct 19, 2022