FDA applicant
Storer Medical Products
FDA records 1 decision for Storer Medical Products (Del Mar, CA) in 1989: 1 510(k) clearance. All are in product code KMO (Binder, Elastic). 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 Storer Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Storer Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Storer Medical Products’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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