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
1369737237
Device Listing 1369737237
Listing Summary
#
Listing key
1369737237
Premarket submission
K170107
Device
Surgi Max Ultra
Applicant
Elliquence, LLC
Product code
GEI
Decision date
2017-05-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
15793
9613563
3002808325
David Lennarz
1
N
2026-01-01
144 Research Drive Hampton VA US 23666