FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P080011
·
Supplement: S158
·
Decision Dec 20, 2023
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- Biofinity Sphere, Biofinity Toric
- PMA Number
- P080011
- Supplement Number
- S158
- 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
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- December 20, 2023
- Date Received
- November 22, 2023
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
upgrades to the software used in the Wet Automated Inspection System for the Biofinity Automated Wet Lines at the CooperVision Manufacturing facility in Puerto Rico
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 |