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
1581187357
Device Listing 1581187357
Listing Summary
#
Listing key
1581187357
Premarket submission
DEN200016
Device
EndoRotor Device
Applicant
Interscope, Inc.
Product code
QNE
Decision date
2020-12-23
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
207453
3011697028
3011697028
INTERSCOPE, INC.
1
N
2026-01-01
200 Commerce Dr. Northbridge MA US 01534