Premarket Approval (PMA)

Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.

• Device: SKINVIVE™ by Juvederm
• Generic Name: Implant, dermal, for aesthetic use
• Applicant: Allergan; 2525 Dupont Dr.; Irvine, CA 92612
• PMA Number: P110033
• Supplement Number: S072
• Date Received: 05/25/2023
• Decision Date: 08/01/2023
• Product Code: LMH
• Advisory Committee: General & Plastic Surgery
• Supplement Type: Normal 180 Day Track No User Fee
• Supplement Reason: Labeling Change - Indications/instructions/shelf life/tradename
• Expedited Review Granted?: No
• Combination Product: Yes
• Predetermined Change Control Plan Authorized: No

Approval Order Statement  
Approval for final revised labeling.