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
1614757848
Device Listing 1614757848
Listing Summary
#
Listing key
1614757848
Premarket submission
K251464
Device
TRI-BEAM PRO, TRI-BEAM (Nd:YAG Laser unit)
Applicant
Jeisys Medical Incorporated
Product code
GEX
Decision date
2025-10-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
331761
3033715699
3033715699
JEISYS MEDICAL NORTH AMERICA INC
1
Y
2026-01-01
70 Blanchard Rd Ste 303 Burlington MA US 01803