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Sculptra

FDA UDI

Class III (US FDA UDI)

by Galderma Laboratories, L.p.

Identity

Trade Name
Sculptra FDA UDI
Generic Name
Dermal tissue reconstructive material, synthetic mineral FDA UDI
Model / Reference
Aesthetic FDA UDI

Identifiers

Primary DI / UDI-DI
20302995961064 FDA UDI
FDA Product Code
LMH FDA UDI
GMDN Term
Dermal tissue reconstructive material, synthetic mineral 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

No

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, synthetic mineral

Sculptra by Galderma Laboratories, L.p. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermal tissue reconstructive material, synthetic mineral.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Galderma Laboratories, L.p.

Sources (1)

  • FDA UDI 036dbf7c-9001-4af1-a2f3-4a9996d42659 33 fields · synced May 30, 2026