Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1620209601
Device Listing 1620209601
Listing Summary
#
Listing key
1620209601
Premarket submission
K032991
Device
LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX
Applicant
Light Age, Inc.
Product code
GEX
Decision date
2004-09-14
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
337030
3015730775
3015730775
LASETECH, LLC
1
N
2026-01-01
11 Princess Road Ste C Lawrenceville NJ US 08648