FDA applicant
Polymer Technology Div. Wilmington Partners, L.P.
FDA records 3 decisions for Polymer Technology Div. Wilmington Partners, L.P. (Rochester, NY) from 1996 to 1999: 3 510(k) clearances. Most are in product codes HQD (Lens, Contact (Other Material) - Daily) and LRX (Case, Contact Lens). Its devices cite 3 predicates, 0 of them its own earlier devices. 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Polymer Technology Div. Wilmington Partners, L.P.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Polymer Technology Div. Wilmington Partners, L.P. since 2007.
Recalls per year
2in 2009
Class I Class II/III not classified
Planning a device like Polymer Technology Div. Wilmington…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Polymer”
FDA records each applicant name separately; these may or may not be the same firm.