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Sign in to claim this brandOMNI INTERNATIONAL CORP.
US
Last updated May 24, 2026
What OMNI INTERNATIONAL CORP. makes
The company manufactures single-use examination and treatment gloves in nitrile, vinyl, and natural rubber (hevea latex) formulations, all non-powdered and non-antimicrobial. It also produces adhesive and non-adhesive bandages, as well as gauze pads in woven and non-woven forms, including non-sterile and non-antimicrobial variants.
These products fall under FDA device classes I and II, with some listed as Class N (no classification required). They are registered in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- omnigloves.com
- —
- —
- [email protected]
- Phone
- +1(603)471-1499
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 079434709
Catalogue (137)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| OmniTrust | 413-02 | FDA UDI | Class I | Active |
| OmniTrust | 413-01 | FDA UDI | Class I | Active |
| OmniTrustTM | 9089-21 | FDA UDI | Class I | Active |
| OmniTrustTM | 50325-19 | FDA UDI | Class I | Active |
| OmniTrustTM | 9061-31 | FDA UDI | Class I | Active |
| OmniTrustTM | 216-23 | FDA UDI | Class I | Active |
| OmniTrustTM | 214-24 | FDA UDI | Class I | Active |
| OmniTrustTM | 9084-52 | FDA UDI | Class I | Active |
| OmniTrustTM | 9062-43 | FDA UDI | Class I | Active |
| OmniTrustTM | 9051-21 | FDA UDI | Class I | Active |
| OmniTrustTM | 9084-21 | FDA UDI | Class I | Active |
| OmniTrustTM | 215-44 | FDA UDI | Class I | Active |
| OmniTrustTM | 201-122 | FDA UDI | Class I | Active |
| OmniTrustTM | 9021-34 | FDA UDI | Class I | Active |
| OmniTrustTM | 214-23 | FDA UDI | Class I | Active |
| OmniTrust | 2155-40 | FDA UDI | Class I | Active |
| OmniTrustTM | 9085-21 | FDA UDI | Class I | Active |
| OmniTrustTM | 215-43 | FDA UDI | Class I | Active |
| OmniTrustTM | 312-14 | FDA UDI | Class I | Active |
| OmniTrustTM | 412-02 | FDA UDI | Class I | Active |
| OmniTrust | 201-125 | FDA UDI | Class I | Active |
| OmniTrustTM | 201-123 | FDA UDI | Class I | Active |
| OmniTrustTM | 113-01 | FDA UDI | Class I | Active |
| OmniTrustTM | 201-121 | FDA UDI | Class I | Active |
| OmniTrustTM | 9012-43 | FDA UDI | Class I | Active |
| OmniTrustTM | 216-24 | FDA UDI | Class I | Active |
| OmniTrust | 217-22 | FDA UDI | Class I | Active |
| OmniTrustTM | 113-04 | FDA UDI | Class I | Active |
| OmniTrush | 201-220 | FDA UDI | Class I | Active |
| OmniTrustTM | 9112-31 | FDA UDI | Class II | Active |
| OmniTrustTM | 9071-80 | FDA UDI | Class I | Active |
| OmniTrustTM | 9084-71 | FDA UDI | Class I | Active |
| OmniTrust | 217-25 | FDA UDI | Class I | Active |
| OmniTrustTM | 204-321 | FDA UDI | Class I | Active |
| OmniTrustTM | 201-124 | FDA UDI | Class I | Active |
| OmniTrustTM | 9083-31 | FDA UDI | Class I | Active |
| OmniTrustTM | 9083-21 | FDA UDI | Class I | Active |
| OmniTrust | 217-23 | FDA UDI | Class I | Active |
| OmniTrustTM | 9084-31 | FDA UDI | Class I | Active |
| OmniTrustTM | 9084-41 | FDA UDI | Class I | Active |
| OmniTrustTM | 203-21 | FDA UDI | Class I | Active |
| OmniTrustTM | 9011-23 | FDA UDI | Class I | Active |
| OmniTrust | 2155-45 | FDA UDI | Class I | Active |
| OmniSafeTM | FAK-0025 | FDA UDI | N | Active |
| OmniTrustTM | 9084-22 | FDA UDI | Class I | Active |
| OmniTrustTM | 9083-71 | FDA UDI | Class I | Active |
| OmniTrustTM | 204-322 | FDA UDI | Class I | Active |
| OmniTrustTM | 213-43 | FDA UDI | Class I | Active |
| OmniTrustTM | 9012-44 | FDA UDI | Class I | Active |
| OmniTrustTM | 313-14 | FDA UDI | Class I | Active |
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