# Prometex, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 4 (1987–1990): 4 510(k) clearances
- Product codes: EBG (2), EWO (1), IWE (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
- K894484: Audiotester Screening Audiometer (Jun 26, 1990)
- K900068: Aristee (Resin, Crown and Bridges) (Apr 3, 1990)
- K892710: Aristee (Temporary Crown & Bridge Resin) (Oct 24, 1989)
- K872894: A2J MZ 44 Laser Light for Positioning (Aug 12, 1987)

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