ClearanceBrief
Company ยท US

Lenstec, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2016. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MSSFolders And Injectors, Intraocular Lens (Iol)5
HQCUnit, Phacofragmentation1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 29, 2016K161776Lenstec LC Injection system
Lenstec, Inc.
MSS
Oct 18, 2013K122848LENSTEC LC INJECTION SYSTEM
Lenstec, Inc.
MSS
Oct 27, 2009K091915FLUID ISOLATION DEVICE
Lenstec, Inc.
HQC
May 7, 2007K063802LENSTEC LC INJECTION SYSTEM
Lenstec, Inc.
MSS
Apr 14, 2006K060533LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM
Lenstec, Inc.
MSS
May 31, 2005K050638LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES
Lenstec, Inc.
MSS

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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