Polymer Technology Div. Wilmington Partners, L.P. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Polymer Technology Div. Wilmington Partners, L.P. - FDA 510(k) Cleare...
3
Total
3
Cleared
0
Denied
Polymer Technology Div. Wilmington Partners, L.P. has 3 FDA 510(k) cleared medical devices. Based in Rochester, US.
Historical record: 3 cleared submissions from 1996 to 1999. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Polymer Technology Div. Wilmington Partners, L.P. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Polymer Technology Div. Wilmington Partners, L.P.
3 devices