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SOFTEC HD POSTERRIOR CHAMBER INTRAOCULAR LENS (PCIOL)

FDA premarket approval P090022/S013 · decided 2012-08-16

Approval details

PMA number
P090022
Supplement
S013
Supplement type
Special (Immediate Track)
Trade name
SOFTEC HD POSTERRIOR CHAMBER INTRAOCULAR LENS (PCIOL)
Generic name
intraocular lens
Applicant
Lenstec, Inc.
Date received
2012-07-24
Decision date
2012-08-16
Days to decision
23 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
APPROVAL FOR A MODIFICATION TO THE DIRECTIONS FOR USE TO INCLUDE A WARNING THAT ENHANCES THE SAFETY IN THE USE OF THE DEVICE.

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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