Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon Toric Aspheric Hydrophobic Acrylic Intraocular Lens
FDA premarket approval P190018/S021 · decided 2022-12-20
Approval details
- PMA number
- P190018
- Supplement
- S021
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon Toric Aspheric Hydrophobic Acrylic Intraocular Lens
- Generic name
- intraocular lens
- Applicant
- Alcon Laboratories, LLC
- Date received
- 2022-11-22
- Decision date
- 2022-12-20
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Fort Worth, TX
- Statement
- Change from two fixtures to a single fixture used for lens cleaning, extraction, vacuum drying and plasma treatment processes.
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