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Softec HD, Sotlec I, Softec HD PS, Softec HDO, Softec HDM

FDA premarket approval P090022/S039 · decided 2021-09-28

Approval details

PMA number
P090022
Supplement
S039
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Softec HD, Sotlec I, Softec HD PS, Softec HDO, Softec HDM
Generic name
intraocular lens
Applicant
Lenstec, Inc.
Date received
2021-09-02
Decision date
2021-09-28
Days to decision
26 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
Use of an alternate lens cleaner in the final cleaning process.

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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