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Juvederm Voluma Xc

FDA UDI

Class III (US FDA UDI)

by Allergan

Identity

Trade Name
JUVEDERM VOLUMA XC FDA UDI
Generic Name
Dermal tissue reconstructive material, microbe-derived, anaesthetic FDA UDI
Device Name
Juvederm Voluma XC 27G 2x1.0mL FDA UDI
Model / Reference
94640 FDA UDI
Description
Juvederm Voluma XC 27G 2x1.0mL FDA UDI

Identifiers

Catalog Number
94640 FDA UDI
Primary DI / UDI-DI
10888628000018 FDA UDI
PMA Number
P110033 FDA UDI
FDA Product Code
LMH FDA UDI
GMDN Term
Dermal tissue reconstructive material, microbe-derived, anaesthetic FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermal tissue reconstructive material, microbe-derived, anaesthetic

Juvederm Voluma Xc by Allergan — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermal tissue reconstructive material, microbe-derived, anaesthetic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allergan

Sources (1)

  • FDA UDI a72edca9-8830-419d-8354-d93dde6bb284 38 fields · synced Jun 8, 2026