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
1054721010
Device Listing 1054721010
Listing Summary
#
Listing key
1054721010
Premarket submission
K080025
Device
LED.L, LED.M, LED.G, LED.B
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.
Product code
EBZ
Decision date
2008-03-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
206786
3011649314
3011649314
PRISMATIK DENTALCRAFT, INC.
1
Y
2026-01-01
2144 Michelson Drive Irvine CA US 92612