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
1138363653
Device Listing 1138363653
Listing Summary
#
Listing key
1138363653
Premarket submission
K093894
Device
ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE
Applicant
Anthogyr
Product code
EFA
Decision date
2010-03-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
40504
8020776
4224
Michael van der Woude
1
N
2020-04-25
2500 Bee Cave Road Bldg 1, Suite 300 Austin TX US 78746