FDA.reportPublic FDA data

Xu Wen

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30183123283018312328Xu Wen1N2026-01-014611 Maydew Mews Way Ellicott MD US 21042
30449059183044905918Xu Wen1N2026-01-014611 Maydew Mews Way Ellicott MD US 21042

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3490381718698662K252345Picosecond Laser Device (PF131-BI)GEX2025-10-23
3490381554638201K251329Diode laser device (RF3120-BI)GEX2025-06-27
2887481447678918K142359Vasc Band hemostatDXC2014-10-23
2887481210863879
3490381441967496
2887481893299526
2887481994836521

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEX22025-10-23
DXC12014-10-23