FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lens, Multifocal Intraocular
PMA: P040020
·
Supplement: S115
·
Decision Aug 25, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Lens, Multifocal Intraocular
- Trade Name
- AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses\s
- PMA Number
- P040020
- Supplement Number
- S115
- Device Class
- FDA Class 3
- Product Code
- MFK
- Generic Name
- Lens, multifocal intraocular
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- August 25, 2025
- Date Received
- July 28, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
the expansion of a clean room for manufacturing for the toric and non-toric Acrysof and Clareon IOLs
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 |
|---|---|---|---|
| MFK | Lens, Multifocal Intraocular | FDA class 3 | Ophthalmic |