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UNIVERDERM

Last updated May 25, 2026

What UNIVERDERM makes

The company produces dermal tissue reconstructive materials, including microbe-derived and synthetic mineral formulations for soft tissue augmentation, as well as anaesthetic-enhanced variants for targeted applications. It also supplies synovial fluid supplementation media for joint lubrication and peripheral intravenous cannulae for vascular access. Examples include hyaluronic acid-based dermal fillers and calcium hydroxylapatite injectables, alongside a synthetic fluid substitute for joint care.

These products are authorised as Class II and Class III medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to domestic regulatory standards for these device classifications.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
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EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 281488639

Catalogue (13)

Device	Model / Reference	Registries	Class	Status
Restylane	Defyne with Lidocaine	FDA UDI	Class III	Active
Juvederm	Voluma	FDA UDI	Class III	Active
Restylane Eyelight	Injectable Gel	FDA UDI	Class III	Active
Juvederm	Volbella	FDA UDI	Class III	Active
Restylane	Lidocaine	FDA UDI	Class III	Active
Synvisc	One	FDA UDI	Class III	Active
Restylane	Lyft Lidocaine	FDA UDI	Class III	Active
Restylane	Refyne with Lidocaine	FDA UDI	Class III	Active
Synvisc	N/A	FDA UDI	Class III	Active
Restylane	Kysse with Lidocaine	FDA UDI	Class III	Active
Bd	Insyte Autoguard Winged	FDA UDI	Class II	Active
Radiesse	Lidocaine	FDA UDI	Class III	Active
Sculptra	N/A	FDA UDI	Class III	Active

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