# Kera Corp.

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 4 (1985–1990): 4 510(k) clearances
- Product codes: HLQ (3), HJB (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
- K901009: Model 2000 Intraoperative Corneascope (May 30, 1990)
- K871479: Videoscan (TM) (May 22, 1987)
- K864037: Kerascan Model 2000 Keratographic Auto Analyzer (Nov 13, 1986)
- K850665: Corneascope Model 1200 (Mar 20, 1985)

Source page: https://510kreport.com/company/kera