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
1991304190
Device Listing 1991304190
Listing Summary
#
Listing key
1991304190
Premarket submission
K171301
Device
Scanmate Flex
Applicant
Dgh Technology, Inc.
Product code
IYO
Decision date
2017-07-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
38352
2522950
2522950
DGH TECHNOLOGY, INC.
1
Y
2026-01-01
110 SUMMIT DR., SUITE B EXTON PA US 19341