Lenstec, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K161776Lenstec LC Injection systemNovember 29, 2016
K122848LENSTEC LC INJECTION SYSTEMOctober 18, 2013
K091915FLUID ISOLATION DEVICEOctober 27, 2009
K063802LENSTEC LC INJECTION SYSTEMMay 7, 2007
K060533LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEMApril 14, 2006
K050638LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSESMay 31, 2005