Omni Intl., Inc.
12 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM (K984066) | Omni Intl., Inc. | 1999-01-13 |
| OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE (K984064) | Omni Intl., Inc. | 1999-01-08 |
| OMNIMED I.V. SOLUTION ADMIN. SET (K853255) | Omni Intl., Inc. | 1985-08-23 |
| OMNIMED SURGICAL GOWN (K851938) | Omni Intl., Inc. | 1985-06-28 |
| OMNIMED CLAMP (K851654) | Omni Intl., Inc. | 1985-05-31 |
| OMNIMED SUPERIOR TRANSDUCER PROTECTOR (K851734) | Omni Intl., Inc. | 1985-05-23 |
| F-SERIES IMPLANT (K850706) | Omni Intl., Inc. | 1985-04-10 |
| OMNIMED IV SOLUTION ADMINISTRATION SET (K850112) | Omni Intl., Inc. | 1985-02-22 |
| OMNIMED NASAL OXYGEN CANNULA (K850066) | Omni Intl., Inc. | 1985-01-24 |
| OMNIPROBE ELECTRICAL NERVE STIMULATOR (K831147) | Omni Intl., Inc. | 1983-07-18 |
| OMNI TENS (K821523) | Omni Intl., Inc. | 1982-06-16 |
| OMNI STIM II (K813604) | Omni Intl., Inc. | 1982-03-08 |
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