FDA applicant
Neitz Instruments Company, Ltd.
FDA records 24 decisions for Neitz Instruments Company, Ltd. (Tokyo, JP) from 1994 to 1997: 24 510(k) clearances. Most are in product codes HLI (Ophthalmoscope, Ac-Powered) and HKM (Retinoscope, Battery-Powered). 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 Neitz Instruments Company, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Neitz Instruments Company, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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