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
1822826212
Device Listing 1822826212
Listing Summary
#
Listing key
1822826212
Premarket submission
K012307
Device
LUXACORE/LUXACORE DUAL
Applicant
Dmg USA, Inc.
Product code
EBF
Decision date
2001-08-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
13630
8044164
3004150030
Pamela Papineau
1
N
2026-01-01
5 WHITCOMB AVENUE Ayer MA US 01432