# Neitz Instruments Company, Ltd.

- Location (FDA's records): Tokyo, JP
- FDA decisions: 24 (1994–1997): 24 510(k) clearances
- Product codes: HLI (7), HKM (5), HLJ (5), HJO (2), HKL (2), HPQ (1), HKI (1), ERA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Heine Optotechnik GmbH & Co. KG: 1 (https://510kreport.com/company/heine-optotechnik)

## Its most-cited devices
- K942712: Neitz Halogen Binocular Indirect Ophthalmoscope IO-a (1994), cited by 1

## Recent decisions
- K972440: Cataractscreener CT - S (Sep 30, 1997)
- K951341: Neitz Slit Lamp SL-H2 (Jun 15, 1995)
- K951337: Fiber Head Light FH-300 (Jun 8, 1995)
- K950788: Otoscope a-34 (May 3, 1995)
- K951340: Neitz Slit Lamp SL-H1 (Apr 10, 1995)
- K951338: Indirect Ophthalmoscope Video System IO0 a TV (Apr 7, 1995)
- K950794: Streak Retinoscope RX-RC (Mar 28, 1995)
- K950791: Streak Retinoscope RX-3 (Mar 28, 1995)

Source page: https://510kreport.com/company/neitz-instruments