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Progenacare Global, LLC

US

Last updated May 30, 2026

What Progenacare Global, LLC makes

Progenacare Global, LLC manufactures animal-derived wound matrix dressings designed for use in wound care applications. These products are intended to support tissue regeneration and promote healing in chronic or acute wounds.

The company’s portfolio is classified under Class II (U) devices in the U.S. and is listed in the FDA’s Unique Device Identifier (UDI) database. The products are regulated under U.S. medical device laws.

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 Progenacare Global, LLC manufacture?

Progenacare Global, LLC specializes in animal-derived wound matrix dressings, which are designed to support tissue regeneration and promote healing in wounds, including chronic or acute cases. These products fall under wound care solutions and are intended for clinical use in medical settings.

Where is Progenacare Global, LLC based?

Progenacare Global, LLC is headquartered in the United States. The company’s operations and regulatory compliance are aligned with U.S. medical device laws, including classification and listing requirements.

Which regulatory registries or databases list Progenacare Global, LLC’s devices?

Progenacare Global, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers and regulators, as required under U.S. medical device regulations.

How are Progenacare Global, LLC’s devices classified in the U.S.?

The company’s wound matrix dressings are classified as Class II (U) devices under U.S. regulations. This classification is based on their intended use in wound care, where they require general controls and special controls to ensure safety and effectiveness, as determined by the FDA.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
770-627-2547
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
054791028

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
ProgenaMatrix PM2012
FDA UDI
UActive
ProgenaMatrix PM3006
FDA UDI
UActive
ProgenaMatrix PM3002
FDA UDI
UActive
ProgenaMatrix PM3010
FDA UDI
UActive
ProgenaMatrix PM3004
FDA UDI
UActive
ProgenaMatrix PM3003
FDA UDI
UActive

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