Surgiplast , Ltd. is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Surgiplast , Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Surgiplast , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Ahmedabad 382 445, IN.
Historical record: 2 cleared submissions from 1995 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Surgiplast , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgiplast , Ltd.
2 devices