Turboseal, L.P. is one of 245 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Turboseal, L.P. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Turboseal, L.P. has 1 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Turboseal, L.P. Filter by specialty or product code using the sidebar.
Turboseal, L.P. — FDA 510(k) Products and Clearance History
1 devices