FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P040045
·
Supplement: S127
·
Decision Sep 22, 2022
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- VISTAKON® (senofilcon A) Brand Contact Lenses
- PMA Number
- P040045
- Supplement Number
- S127
- Device Class
- FDA Class 3
- Product Code
- LPM
- Generic Name
- Lenses, soft contact, extended wear
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 22, 2022
- Date Received
- June 24, 2022
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for a change to the material of the lens container closure (foil lidstock) for VISTAKON® (etafilcon A) and (senofilcon A) Brand Contact Lenses.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LPM | Lenses, Soft Contact, Extended Wear | FDA class 3 | Ophthalmic |