RHA® Redensity, RHA ®2, RHA ®3, RHA ®4 dermal fillers
FDA premarket approval P170002/S025 · decided 2023-01-26
Approval details
- PMA number
- P170002
- Supplement
- S025
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- RHA® Redensity, RHA ®2, RHA ®3, RHA ®4 dermal fillers
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Teoxane S.A.
- Date received
- 2022-12-27
- Decision date
- 2023-01-26
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Geneva
- Statement
- Manufacturing change to increase the mixing batch size from 12L to 24L.
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