# Ormed Mfg., Inc.

- Location (FDA's records): Buffalo, NY
- FDA decisions: 23 (1983–1994): 23 510(k) clearances
- Product codes: EFQ (14), GDY (3), KDC (2), BXB (1), KDD (1), GDI (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
- K931555: Artromot K2 CPM (Jan 31, 1994)
- K882529: Butcher Strung Tonsil Sponge (Jul 18, 1988)
- K882528: Cylindrical Sponge (Jul 18, 1988)
- K882527: Gauze Sponge (Jul 18, 1988)
- K882530: Tape Strung Tonsil Sponge (Jul 18, 1988)
- K880909: Tracheotomy Sponges (Mar 17, 1988)
- K880854: Strung Absorbent Balls (Mar 17, 1988)
- K880852: Rosebud Dissectors (Mar 17, 1988)

Source page: https://510kreport.com/company/ormed-mfg