Atlas FDA

LENSTEC SOFTEC HD PCIOL

FDA premarket approval P090022/S014 · decided 2012-09-20

Approval details

PMA number
P090022
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
LENSTEC SOFTEC HD PCIOL
Generic name
intraocular lens
Applicant
Lenstec, Inc.
Date received
2012-08-27
Decision date
2012-09-20
Days to decision
24 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
INCLUSION OF TWO ADDITIONAL STEAM STERILIZER UNITS FOR THE STERILIZATION OF THE FIRM'S SOFTEC SERIES OF IOLS.

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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