# Technitex, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 3 (1988–1989): 3 510(k) clearances
- Product codes: HLR (1), HJA (1), HLP (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
- K893968: VKG 2000 Video Keratometer (Sep 11, 1989)
- K883471: VKG 1000, Video Keratometer (Nov 8, 1988)
- K882902: QRK 100, Qualitative Ring Keratoscope (Aug 4, 1988)

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