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
1141934075
Device Listing 1141934075
Listing Summary
#
Listing key
1141934075
Premarket submission
K151485
Device
GENESIS
Applicant
Dornier Medtech America, Inc.
Product code
JAA
Decision date
2015-06-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9285
9611388
3002806833
John Hoffer
1
N
2026-01-01
1155 Roberts Blvd Nw KENNESAW GA US 30144