FDA applicant
Storz Instrument Co.
FDA records 101 decisions for Storz Instrument Co. (St. Louis, MO) from 1976 to 1998: 101 510(k) clearances. Most are in product codes HQC (Unit, Phacofragmentation) and HQE (Instrument, Vitreous Aspiration And Cutting…). Its devices cite 29 predicates, 21 of them its own earlier devices. 8 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Storz Instrument Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Storz Instrument Co. since 2007.
Recalls per year
3in 2010
Class I Class II/III not classified
Planning a device like Storz Instrument Co.’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 “Storz”
FDA records each applicant name separately; these may or may not be the same firm.