FDA applicant
Medical Products Div.
FDA records 1 decision for Medical Products Div. (Indianapolis, IN) in 2006: 1 510(k) clearance. All are in product code HIB (Speculum, Vaginal, Nonmetal). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Medical Products Div.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medical Products Div. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medical Products Div.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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