# Promedex, Inc.

- Location (FDA's records): Fort Woth, TX
- FDA decisions: 3 (1990–1991): 3 510(k) clearances
- Product codes: MFD (1), KYA (1), HQY (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
- K914407: Promoglass (TM) Sunglasses (Non-Prescription) (Dec 31, 1991)
- K905764: Seminor (Mar 12, 1991)
- K900404: Varicoscreen (TM) (Dec 7, 1990)

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