Atlas FDA

Juvederm Voluma XC

FDA premarket approval P110033/S042 · decided 2019-08-29

Approval details

PMA number
P110033
Supplement
S042
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Juvederm Voluma XC
Generic name
Implant, dermal, for aesthetic use
Applicant
Allergan
Date received
2019-02-28
Decision date
2019-08-29
Days to decision
182 days
Decision code
APPR
Product code
LMH
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Irvine, CA
Statement
Approval for an update to the labeling for Juvederm Voluma XC to include the use of cannula.

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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