ClearanceBrief
Company ยท US

Light Age, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2012. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument6
PDZLasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 3, 2012K113115EPICARE YAG
Light Age, Inc.
GEX
Sep 15, 2011K110370Q-CLEAR
Light Age, Inc.
PDZ
Nov 3, 2009K091625EPICARE-DUO LASER SYSTEM
Light Age, Inc.
GEX
Sep 14, 2004K032991LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX
Light Age, Inc.
GEX
Feb 25, 2004K033259LIGHT AGE Q-CLEAR LASER, MODEL 701-1101
Light Age, Inc.
GEX
Jan 7, 1999K983977LIGHT AGE EPICARE ALEXANDRITE LASER
Light Age, Inc.
GEX
Feb 17, 1998K980131ALEX TA2 ERASER
Light Age, Inc.
GEX

Latest recalls

DateFirm and productCodeLinked 510(k)
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