FDA applicant
Medical Instrument Development Laboratories, Inc.
FDA records 23 decisions for Medical Instrument Development Laboratories, Inc. (San Leandro, CA) from 1982 to 2016: 23 510(k) clearances. Most are in product codes HQE (Instrument, Vitreous Aspiration And Cutting…) and HQC (Unit, Phacofragmentation). Its devices cite 5 predicates, 5 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Medical Instrument Development Laboratories”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Medical Instrument Development Laboratories, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
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