# Gyne-Tech Instrument Corp.

- Location (FDA's records): Burbank, CA
- FDA decisions: 3 (1992–1996): 3 510(k) clearances
- Product codes: HGI (1), GEX (1), GEH (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
- K954911: Omega Ultrascan (Jan 24, 1996)
- K922878: Model GT1ST Cryosurgical Instrument (Sep 2, 1992)
- K914367: Electrosurgical Generator Model ESU100/250/550 (Apr 28, 1992)

Source page: https://510kreport.com/company/gyne-tech-instrument