Belotero Balance + Lidocaine Dermal Filler, Belotero Balance Dermal Filler
FDA premarket approval P090016/S045 · decided 2021-12-08
Approval details
- PMA number
- P090016
- Supplement
- S045
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Belotero Balance + Lidocaine Dermal Filler, Belotero Balance Dermal Filler
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Merz North America, Inc.
- Date received
- 2021-05-05
- Decision date
- 2021-12-08
- Days to decision
- 217 days
- Decision code
- APPR
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Franksville, WI
- Statement
- Approval for a change from traditional sterility testing to parametric release strategy for product release of Belotero Balance (BB) and Belotero Balance + Lidocaine (BBL).
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| DESCRIBE PFD Patch (K172689) | Merz North America, Inc. | 2017-11-29 |