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US
Last updated May 30, 2026
What Poss, LLC makes
Poss, LLC manufactures single-use nitrile examination and treatment gloves without powder or antimicrobial additives, designed for medical and procedural use. They also produce disposable surgical gowns intended for sterile barrier protection during surgical and clinical procedures.
The company’s products are regulated under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Poss, LLC 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 Poss, LLC manufacture?
Poss, LLC specializes in single-use medical devices, specifically nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, as well as disposable surgical gowns. These products are designed for medical and procedural use, including sterile barrier protection during surgical and clinical procedures. The focus on nitrile gloves and gowns reflects their role in infection control and patient safety.
Where is Poss, LLC based, and how does that affect its devices?
Poss, LLC is based in the United States, which means its devices are subject to U.S. regulatory requirements, including those set by the FDA. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations. The location also influences market access and distribution channels.
Which regulatory registries or databases list Poss, LLC’s devices?
Poss, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track medical devices throughout their distribution and helps ensure transparency, traceability, and compliance with regulatory requirements. This listing is essential for healthcare providers and regulators to identify and verify the devices in use.
How are Poss, LLC’s devices classified under FDA regulations?
Poss, LLC’s devices fall into two main FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional controls to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body’s interaction with it, such as gloves and gowns designed for sterile procedures.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- possmedical.com
- —
- —
- [email protected]
- Phone
- 850-661-4197
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 066882769
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Resist | RST200 | FDA UDI | Class I | Active |
| Assure Plus | ASRP100 | FDA UDI | Class I | Active |
| POSS Medical | E104170 | FDA UDI | Class II | Active |
| POSS Medical | P103150 | FDA UDI | Class II | Active |
| Assure Plus | ASRP300 | FDA UDI | Class I | Active |
| Assure | ASR350 | FDA UDI | Class I | Active |
| Resist | RST300 | FDA UDI | Class I | Active |
| Assure | ASR200 | FDA UDI | Class I | Active |
| Resist | RST100 | FDA UDI | Class I | Active |
| POSS Medical | P103170 | FDA UDI | Class II | Active |
| Resist | RST350 | FDA UDI | Class I | Active |
| Assure | ASR300 | FDA UDI | Class I | Active |
| Assure | ASR100 | FDA UDI | Class I | Active |
| Assure Plus | ASRP350 | FDA UDI | Class I | Active |
| Assure Plus | ASRP200 | FDA UDI | Class I | Active |
| POSS Medical | P103160 | FDA UDI | Class II | Active |
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