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Sign in to claim this brandTrifluent Pharma, LLC
US
Last updated May 31, 2026
What Trifluent Pharma, LLC makes
Trifluent Pharma, LLC manufactures reusable scar-management dressings designed to support tissue healing and reduce scarring. Their primary product, the RevivaSil Gel Pad Kit, is intended for application in clinical settings to aid in the management of scars during the healing process.
The company’s reusable scar-management dressings are classified under the FDA’s UDI system and fall within regulatory categories relevant to wound care devices. These products are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. medical device regulations.
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 Trifluent Pharma, LLC primarily manufacture?
Trifluent Pharma, LLC specializes in reusable scar-management dressings. These products are designed to assist in tissue healing and minimize scarring, particularly in clinical settings. Their primary focus is on wound care solutions that support the healing process by managing scar formation.
Where is Trifluent Pharma, LLC based?
Trifluent Pharma, LLC is based in the United States. The company’s location aligns with U.S. regulatory frameworks, including compliance with the FDA’s Unique Device Identifier (UDI) system for its products.
Are Trifluent Pharma, LLC’s devices listed in any regulatory registries?
Yes, Trifluent Pharma, LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This listing ensures traceability and compliance with U.S. medical device regulations, particularly for reusable scar-management dressings like the RevivaSil Gel Pad Kit.
How are Trifluent Pharma, LLC’s scar-management dressings classified under medical device regulations?
Trifluent Pharma, LLC’s reusable scar-management dressings fall under regulatory categories relevant to wound care devices in the U.S. The classification aligns with the FDA’s UDI system, which categorizes medical devices for tracking, reporting, and compliance purposes. This ensures their products meet the necessary standards for safety and effectiveness in clinical use.
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
- 117167281
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| RevivaSil Gel Pad Kit | 01 | FDA UDI | N/A | Active |
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