# Reichert Ophthalmic Instruments, Div. Leica, Inc.

- Location (FDA's records): Depew, NY
- FDA decisions: 3 (1994–2000): 3 510(k) clearances
- Product codes: HKX (1), HLQ (1), HKY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K000288: Reichert CT200 Contact Tonometer (Mar 23, 2000)
- K964290: Eyechek (Jan 9, 1997)
- K941865: Xpert NCT (Sep 29, 1994)

Source page: https://510kreport.com/company/reichert-ophthalmic-instruments-div-leica