FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P080011
·
Supplement: S134
·
Decision Nov 19, 2021
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- Biofinity XR Toric; Biofinity Toric Multifocal
- PMA Number
- P080011
- Supplement Number
- S134
- 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
- November 19, 2021
- Date Received
- October 28, 2021
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Removal of the measurement of the junction thickness from the Biofinity MTO (Made To Order) Manufacturing Process at the CooperVision Manufacturing, Ltd. facility in Hamble, United Kingdom.
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 |