FDA.reportPublic FDA data

LASETECH, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30157307753015730775LASETECH, LLC1N2026-01-0111 Princess Road Ste C Lawrenceville NJ US 08648

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
G760504ZTH0EpiCare-Zenith - Dual laser 755nm Alexandrite and 1064nm Nd:YAG medical laser with primary use for hair removal.609-450-1866gabriel.nunez@lasetech.com
G760504ZTHA0EpiCare-Zenith - Medical laser system utilizing a 755nm Alexandrite laser, primarily used for hair removal.609-450-1866gabriel.nunez@lasetech.com
G760504ZTHY0EpiCare-Zenith - Medical laser system utilizing a 1064nm Nd:YAG laser, primarily used for hair removal.609-450-1866gabriel.nunez@lasetech.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3370302001220813K983977LIGHT AGE EPICARE ALEXANDRITE LASERGEX1999-01-07
3370301852720942K980131ALEX TA2 ERASERGEX1998-02-17
3370301628655230K113115EPICARE YAGGEX2012-04-03
3370301512582928K091625EPICARE-DUO LASER SYSTEMGEX2009-11-03
3370301620209601K032991LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPXGEX2004-09-14

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEX52012-04-03

GUDID#