Is this your brand? Sign in to claim ownership.
Sign in to claim this brandMohawk Hospital Equipment, Inc.
US
Last updated May 24, 2026
What Mohawk Hospital Equipment, Inc. makes
Mohawk Hospital Equipment, Inc. manufactures nitrile and vinyl examination and treatment gloves, both non-powdered. The nitrile gloves are also non-antimicrobial, designed for medical procedures requiring barrier protection. The company produces these gloves under the RISERVA brand.
These products fall under Class I regulatory classification in the U.S. and are listed in the FDA’s Unique Device Identifier (UDI) database. 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.
Frequently asked questions
What types of medical devices does Mohawk Hospital Equipment, Inc. manufacture?
Mohawk Hospital Equipment, Inc. specializes in manufacturing nitrile and vinyl examination and treatment gloves. The nitrile gloves are specifically designed as non-powdered and non-antimicrobial, intended for medical procedures where barrier protection is required. These gloves are branded under the RISERVA name.
Where is Mohawk Hospital Equipment, Inc. based?
Mohawk Hospital Equipment, Inc. is based in the United States. The company’s headquarters and operations are located within the country.
Which regulatory registries or databases list Mohawk Hospital Equipment, Inc.’s devices?
Mohawk Hospital Equipment, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S.
How are Mohawk Hospital Equipment, Inc.’s devices classified under U.S. regulations?
Mohawk Hospital Equipment, Inc.’s gloves fall under Class I regulatory classification in the U.S. This classification is typically assigned to low-risk medical devices that pose minimal potential harm to users. The classification is based on the device’s intended use and risk profile.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 013326384
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Riserva | BASVGPF40031 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40011 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40022 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30022 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40041 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30021 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40042 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30042 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30042 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40021 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40032 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30031 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30011 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30021 | FDA UDI | Class I | Active |
| Riserva | BASNGPF30012 | FDA UDI | Class I | Active |
| Riserva | BASVGPF40012 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.