# Bentec Medical, Inc.

- Location (FDA's records): Sacramento, CA
- FDA decisions: 3 (1997–2001): 3 510(k) clearances
- Product codes: EWD (1), EMX (1), FGE (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
- K002650: Van Andle Dilation, Emerald Guidewire, Model VAD6, 502-726 (Feb 16, 2001)
- K971411: Disposable Silicone Epistaxis Catheter V-27030/Disposable Silicone Epistaxis Catheter Kit V-27030K (Jun 3, 1997)
- K971517: Silicone Putty Ear Plugs (Jun 2, 1997)

Source page: https://510kreport.com/company/bentec-medical