# Omni Intl., Inc.

- Location (FDA's records): Palm Springs, CA
- FDA decisions: 12 (1982–1999): 12 510(k) clearances
- Product codes: GZJ (2), FPA (2), KGO (2), FIB (1), CAT (1), FYA (1), HXD (1), DZE (1), IPF (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
- K984066: Omnigrip, Latex Surgical Glove, Powder-Free with Protein Labeling Claim (Jan 13, 1999)
- K984064: Omnigrip, Latex Surgical Glove, Powder Free (Jan 8, 1999)
- K853255: Omnimed I.V. Solution Admin. Set (Aug 23, 1985)
- K851938: Omnimed Surgical Gown (Jun 28, 1985)
- K851654: Omnimed Clamp (May 31, 1985)
- K851734: Omnimed Superior Transducer Protector (May 23, 1985)
- K850706: F-Series Implant (Apr 10, 1985)
- K850112: Omnimed IV Solution Administration Set (Feb 22, 1985)

Source page: https://510kreport.com/company/omni-intl