Atlas FDA

SBL-3 Multifocal Intraocular Lens

FDA premarket approval P200020 · decided 2022-07-22

Approval details

PMA number
P200020
Trade name
SBL-3 Multifocal Intraocular Lens
Generic name
Lens, multifocal intraocular
Applicant
Lenstec, Inc.
Date received
2020-03-16
Decision date
2022-07-22
Days to decision
858 days
Decision code
APPR
Product code
MFK
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
Approval for the Lenstec SBL-3 Multifocal Intraocular Lens. This Lenstec SBL-3 Multifocal Intraocular Lens is indicated for primary implantation for the visual correction of aphakia, in adult patients with 1 diopter or less of pre-existing corneal astigmatism, in whom a cataractous lens has been removed. The lens mitigates the effects of presbyopia by providing a bifocal correction. Compared to an aspheric monofocal IOL, the lens provides improved near visual acuity, while maintaining comparable

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510(k) clearances by this applicant

RecordFirmDate
Lenstec LC Injection system (K161776)Lenstec, Inc.2016-11-29
LENSTEC LC INJECTION SYSTEM (K122848)Lenstec, Inc.2013-10-18
FLUID ISOLATION DEVICE (K091915)Lenstec, Inc.2009-10-27
LENSTEC LC INJECTION SYSTEM (K063802)Lenstec, Inc.2007-05-07
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM (K060533)Lenstec, Inc.2006-04-14
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES (K050638)Lenstec, Inc.2005-05-31