FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Lens

PMA: P840060 · Supplement: S049 · Decision Dec 2, 2021
Classifications
1
FEI Numbers
59
Registration Numbers
59

Basic Information

Device Name
Intraocular Lens
Trade Name
Single-Piece PMMA Posterior Chamber IOL
PMA Number
P840060
Supplement Number
S049
Device Class
FDA Class 3
Product Code
HQL
Generic Name
intraocular lens
Regulation Number
886.3600
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
December 2, 2021
Date Received
June 21, 2021
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for a manufacturing site located at PT. CIBA VISION Batam located at Jalan Beringin Kav. #204, Batamindo Industrial Park, Muka Kuning Batam Island, 29433 Indonesia for manufacturing, packaging, and sterilization.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HQL Intraocular Lens