FDA.reportPublic FDA data

Xintec-Corp

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
29388892938889XINTEC CORPORATION1N2026-01-011660 SOUTH LOOP ROAD ALAMEDA CA US 94502

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
392361809019470K951910ODYSSEY HO:YAG SURGICAL LASER SYSTEMS & ACCESSORIESGEX1995-12-27
392361562242415K951760OPTILITE VIII LASER SURGERY ACCESSORIESGEX1995-11-29
392361522945363K211517Optica XT Thulium Fiber Laser and Accessories, also known as Optica XT, Optica XT Thulium Fiber Laser, Thulium Fiber Laser 1940 nm, Optica XT Thulium Fiber Laser 1940 nm, Optica XT 60 Thulium Fiber Laser 1940 nm, Optica XT Superpulse Thulium Fiber Laser 1940 nm, OptiLITE Laser Fibers and AccessoriesGEX2021-11-09
392361477419009K082230VECTRA PLUS LASER SYSTEM AND ACCESSORIESGEX2010-02-03

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEX42021-11-09

PMN#