Atlas FDA

Belotero Balance Dermal Filler, Belotero Balance (+) Lidocaine Dermal Filler

FDA premarket approval P090016/S061 · decided 2024-10-02

Approval details

PMA number
P090016
Supplement
S061
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Belotero Balance Dermal Filler, Belotero Balance (+) Lidocaine Dermal Filler
Generic name
Implant, dermal, for aesthetic use
Applicant
Merz North America, Inc.
Date received
2024-09-04
Decision date
2024-10-02
Days to decision
28 days
Decision code
OK30
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Franksville, WI
Statement
a modification to the QC final acceptance process for Belotero Balance brand dermal fillers

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510(k) clearances by this applicant

RecordFirmDate
DESCRIBE PFD Patch (K172689)Merz North America, Inc.2017-11-29