Atlas FDA

Skinvive by Juvéderm

FDA premarket approval P110033/S059 · decided 2023-05-11

Approval details

PMA number
P110033
Supplement
S059
Supplement type
Panel Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Skinvive by Juvéderm
Generic name
Implant, dermal, for aesthetic use
Applicant
Allergan
Date received
2021-02-24
Decision date
2023-05-11
Days to decision
806 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Irvine, CA
Statement
Approval for SKINVIVE™ by JUVÉDERM® injectable gel, indicated for intradermal injection to improve facial skin smoothness of the cheeks in adults over the age of 21.

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510(k) clearances by this applicant

RecordFirmDate
NATRELLE INSPIRA Single Use Sizers for Gel Implants (K203229)Allergan2021-06-02
TrueTear Intranasal Tear Neurostimulator (K193589)Allergan2020-08-31
Natrelle 133 Plus MICROCELL Tissue Expander (K180826)Allergan2018-12-21
Natrelle 133S Tissue Expander (K182054)Allergan2018-08-29
TrueTear Intranasal Tear Neurostimulator (DEN170086)Allergan2018-05-17
SERI SURGICAL SCAFFOLD (K123128)Allergan2013-04-25