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Sign in to claim this brandLifeguard Inc.
US
Last updated May 27, 2026
What Lifeguard Inc. makes
Lifeguard Inc. manufactures single-use examination and treatment gloves made from nitrile, hevea latex, and vinyl. The gloves are produced in non-powdered and non-antimicrobial versions, designed for medical and clinical use. These products are intended for procedures requiring barrier protection against pathogens and contaminants.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. These devices are regulated under the US Food and Drug Administration’s requirements for general controls and are intended for distribution within 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 Lifeguard Inc. manufacture?
Lifeguard Inc. specializes in single-use examination and treatment gloves for medical and clinical use. Their product line includes gloves made from nitrile, hevea latex, and vinyl, all produced in non-powdered and non-antimicrobial versions. These gloves are designed to provide barrier protection against pathogens and contaminants during medical procedures.
Where is Lifeguard Inc. based, and where are their devices primarily used?
Lifeguard Inc. is based in the United States. Their devices are intended for distribution within the US and are regulated under the FDA’s requirements for medical devices. The company’s focus on Class I devices aligns with the FDA’s general controls framework, which applies to low-risk products like examination gloves.
How are Lifeguard Inc.’s devices classified by regulatory authorities?
Lifeguard Inc.’s gloves fall under the FDA’s Class I medical device classification. This classification is assigned to devices posing minimal risk to patients, such as single-use examination gloves, which are subject to general controls (e.g., manufacturing practices, labeling) rather than strict pre-market approval. The classification reflects their intended use for barrier protection without invasive procedures.
Are Lifeguard Inc.’s devices listed in any regulatory registries?
Yes, Lifeguard Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and transparency in the supply chain for medical devices regulated by the FDA. Listing in this database helps healthcare providers and regulators verify product details, such as manufacturer information and device identifiers.
Why are Lifeguard Inc.’s gloves categorized as non-powdered and non-antimicrobial?
Lifeguard Inc.’s gloves are designed as non-powdered to avoid potential inhalation risks (e.g., latex powder) during medical procedures, which could cause allergic reactions or respiratory issues. They are also non-antimicrobial to prevent unintended resistance development in pathogens while still providing reliable barrier protection. This formulation aligns with clinical preferences for gloves that minimize additional chemical exposure without compromising safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 122173023
Catalogue (44)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Life Guard | 6334 | FDA UDI | Class I | Active |
| Life Guard | 6355 | FDA UDI | Class I | Active |
| Life Guard | 2322 | FDA UDI | Class I | Active |
| Life Guard | 1262 | FDA UDI | Class I | Active |
| Life Guard | 2325 | FDA UDI | Class I | Active |
| Life Guard | 6333 | FDA UDI | Class I | Active |
| Life Guard | 1264 | FDA UDI | Class I | Active |
| Life Guard | 2323 | FDA UDI | Class I | Active |
| Life Guard | 6394W | FDA UDI | Class I | Active |
| Life Guard | 6302 | FDA UDI | Class I | Active |
| Life Guard | 6304 | FDA UDI | Class I | Active |
| Life Guard | 2324 | FDA UDI | Class I | Active |
| Life Guard | 6344 | FDA UDI | Class I | Active |
| Life Guard | 6345 | FDA UDI | Class I | Active |
| Life Guard | 6305 | FDA UDI | Class I | Active |
| Life Guard | 6374 | FDA UDI | Class I | Active |
| Life Guard | 6373 | FDA UDI | Class I | Active |
| Life Guard | 1202 | FDA UDI | Class I | Active |
| Life Guard | 6376 | FDA UDI | Class I | Active |
| Life Guard | 6301 | FDA UDI | Class I | Active |
| Life Guard | 1263 | FDA UDI | Class I | Active |
| Life Guard | 6353 | FDA UDI | Class I | Active |
| Life Guard | 2302 | FDA UDI | Class I | Active |
| Life Guard | 6346 | FDA UDI | Class I | Active |
| Life Guard | 1261 | FDA UDI | Class I | Active |
| Life Guard | 6343 | FDA UDI | Class I | Active |
| Life Guard | 6352 | FDA UDI | Class I | Active |
| Life Guard | 6303 | FDA UDI | Class I | Active |
| Life Guard | 6332 | FDA UDI | Class I | Active |
| Life Guard | 2304 | FDA UDI | Class I | Active |
| Life Guard | 6393W | FDA UDI | Class I | Active |
| Life Guard | 1204 | FDA UDI | Class I | Active |
| Life Guard | 6354 | FDA UDI | Class I | Active |
| Life Guard | 6395W | FDA UDI | Class I | Active |
| Life Guard | 1203 | FDA UDI | Class I | Active |
| Life Guard | 2303 | FDA UDI | Class I | Active |
| Life Guard | 1265 | FDA UDI | Class I | Active |
| Life Guard | 6375 | FDA UDI | Class I | Active |
| Life Guard | 2305 | FDA UDI | Class I | Active |
| Life Guard | 1205 | FDA UDI | Class I | Active |
| Life Guard | 6372 | FDA UDI | Class I | Active |
| Life Guard | 6392W | FDA UDI | Class I | Active |
| Life Guard | 6342 | FDA UDI | Class I | Active |
| Life Guard | 6335 | FDA UDI | Class I | Active |
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