Identity
- Trade Name
- Radiesse Volume Advantage 1.5cc FDA UDI
- Generic Name
- Dermal tissue reconstructive material, synthetic mineral FDA UDI
- Device Name
- Radiesse Injectable Implant is a volumizing filler indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds and it is also intended for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus. Radiesse Volumizing Filler Kit contains (1) injectable implant and (2) 27 gauge thin walled x 0.75 inch needles. FDA UDI
- Model / Reference
- 8071M0K1 FDA UDI
- Description
- Radiesse Injectable Implant is a volumizing filler indicated for subdermal implantation for the correction of moderate to severe facial wrinkles and folds, such as nasolabial folds and it is also intended for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus. Radiesse Volumizing Filler Kit contains (1) injectable implant and (2) 27 gauge thin walled x 0.75 inch needles. FDA UDI
Identifiers
- Primary DI / UDI-DI
- M2138071M0K15 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Dimensions & Sizes
- Size
- Total Volume — 1.5 Milliliter FDA UDI
Category: Dermal tissue reconstructive material, synthetic mineral
Radiesse Volume Advantage 1.5cc by Merz North America, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dermal tissue reconstructive material, synthetic mineral.
- Sculptra — GALDERMA LABORATORIES, L.P. · Class III
- Sculptra — UNIVERDERM · Class III
- Sculptra — GALDERMA LABORATORIES, L.P. · Class III
- Sculptra — Qmed, Inc. · Class III
- Sculptra — GALDERMA LABORATORIES, L.P. · Class III
- Sculptra — GALDERMA LABORATORIES, L.P. · Class III
- Sculptra — GALDERMA LABORATORIES, L.P. · Class III
- Sculptra — Qmed, Inc. · Class III
Cleared under the same submission
P050037 also covers:
P050052 also covers:
- Radiesse (+) Lidocaine — Merz North America, Inc.
- Radiesse (+) Lidocaine 0.8cc Injectable Implant — Merz North America, Inc.
- Radiesse (+) Lidocaine1.5cc Injectable Implant — Merz North America, Inc.
- Radiesse Moderate Fill 0.8cc — Merz North America, Inc.
- Radiesse Volume Advantage — Merz North America, Inc.
- Radiesse Volume Advantage 1.5cc — Merz North America, Inc.
- Radiesse — UNIVERDERM
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Merz North America, Inc.
Sources (1)
- FDA UDI eaeaa8ee-a66a-4209-a796-a096a6b17efe 37 fields · synced Jun 9, 2026