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Meddcare Corporation

US

Last updated May 24, 2026

What Meddcare Corporation makes

Meddcare Corporation manufactures non-powdered vinyl examination and treatment gloves, as well as nitrile surgical gloves designed for medical use. These products are intended for single-use procedures to maintain hygiene and reduce contamination risk during clinical examinations and surgical interventions.

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. The products are regulated under US medical device laws, with compliance requirements applicable to their designated categories.

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 Meddcare Corporation manufacture?

Meddcare Corporation specializes in single-use medical gloves, specifically non-powdered vinyl examination and treatment gloves, as well as nitrile surgical gloves. These products are designed to maintain hygiene and minimize contamination risk during clinical examinations and surgical procedures.

Where is Meddcare Corporation based?

Meddcare Corporation is based in the United States. The company’s products are developed and manufactured in compliance with US medical device regulations.

Which regulatory registries list Meddcare Corporation’s devices?

Meddcare Corporation’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 US, ensuring traceability and compliance with regulatory requirements.

How are Meddcare Corporation’s devices classified under FDA regulations?

Meddcare Corporation’s products fall under FDA’s Class I medical device classification. This classification applies to devices posing minimal risk, where general controls (such as good manufacturing practices) are sufficient for regulatory oversight. The company’s gloves are regulated under US medical device laws applicable to their specific categories.

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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LinkedIn
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Facebook
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Email
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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
108618903

Catalogue (20)

DeviceModel / ReferenceRegistriesClassStatus
Best Care BCGN447-XL
FDA UDI
Class IActive
Best Care BCGN447-S
FDA UDI
Class IActive
Best Care BCGPV447-M
FDA UDI
Class IActive
Best Care BCGVEX447-XL
FDA UDI
Class IActive
Best Care BCGVEX447-S
FDA UDI
Class IActive
Best Care BCGN447-M
FDA UDI
Class IActive
Best Care BCGN447-XL
FDA UDI
Class IActive
Best Care BCGN447-L
FDA UDI
Class IActive
Best Care BCGVEX447-M
FDA UDI
Class IActive
Best Care BCGVEX447-L
FDA UDI
Class IActive
Best Care BCGPV447-L
FDA UDI
Class IActive
Best Care BCGN447-M
FDA UDI
Class IActive
Best Care BCGVEX447-M
FDA UDI
Class IActive
Best Care BCGN447-S
FDA UDI
Class IActive
Best Care BCGPV447-S
FDA UDI
Class IActive
Best Care BCGVEX447-XL
FDA UDI
Class IActive
Best Care BCGVEX447-L
FDA UDI
Class IActive
Best Care BCGVEX447-S
FDA UDI
Class IActive
Best Care BCGPV447-XL
FDA UDI
Class IActive
Best Care BCGN447-L
FDA UDI
Class IActive

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