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Softec HD, Softec I, Softec HD PS, Softec HDO, and Softec HDM IOLs

FDA premarket approval P090022/S038 · decided 2021-01-07

Approval details

PMA number
P090022
Supplement
S038
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Softec HD, Softec I, Softec HD PS, Softec HDO, and Softec HDM IOLs
Generic name
intraocular lens
Applicant
Lenstec, Inc.
Date received
2020-12-11
Decision date
2021-01-07
Days to decision
27 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
Introduction of two additional steam sterilizers into the existing sterilization process of Lenstec's HEMA intraocular lenses.

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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