# Biomed Devices Corp.

- Location (FDA's records): Grand Junction, CO
- FDA decisions: 2 (1997–1997): 2 510(k) clearances
- Product codes: LPL (2)
- 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
- K971515: Promed 38 Sofblu (Polymacon) Soft (Spherical & Toric) Daily Wear Contact Lens (Tinted, Lathe-Cut Form Lens Blank) (May 20, 1997)
- K970615: Promed 55-G Soft Daily Wear Contact Lens (Mar 19, 1997)

Source page: https://510kreport.com/company/biomed-devices