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
1462251726
Device Listing 1462251726
Listing Summary
#
Listing key
1462251726
Premarket submission
K081015
Device
CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
Applicant
Biolitec, Inc.
Product code
GEX
Decision date
2008-07-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
347479
3043657394
3043657394
Wen Xu
1
N
2026-01-01
4611 Maydew Mews Way Ellicott City MD US 21042