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FDA 510(k) Applications Submitted by LENSTEC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091915
06/30/2009
FLUID ISOLATION DEVICE
LENSTEC, INC.
K122848
09/18/2012
LENSTEC LC INJECTION SYSTEM
LENSTEC, INC.
K063802
12/22/2006
LENSTEC LC INJECTION SYSTEM
LENSTEC, INC.
K060533
02/28/2006
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM
LENSTEC, INC.
K050638
03/11/2005
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES
LENSTEC, INC.
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