FDA applicant
Innovative Products Mfg.
FDA records 1 decision for Innovative Products Mfg. (East Haven, CT) in 1990: 1 510(k) clearance. All are in product code EAK (Screen, Leaded, Operator Radiation Protector). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Innovative Products Mfg.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Innovative Products Mfg. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Innovative Products Mfg.’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) Report