# INTERSCOPE, INC.

FEI: 3011697028
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: INTERSCOPE., INC (#10054826)

Address: 200 Commerce Dr., Northbridge, MA, US



## Products

Total registered: 1
Top product codes: PTE
Regulation §: 884.1690

Proprietary names: 3.2-EPR-EGD-F EndoRotor® 3.2mm Endoscopic Powered Resection (EPR) Catheter – Gastroscope Fuji, 3.2-EPR-EGD-OP EndoRotor® 3.2mm Endoscopic Powered Resection (EPR) Catheter – Gastroscope Olympus/Pentax, 6-EPR-EGD EndoRotor® 6mm Endoscopic Powered Resection (EPR) Catheter, CATHGUIDE EndoRotor® Catheter Guide, ESS-CONSOLE EndoRotor® EndoSurgery System - Console, EPR-TRAP EndoRotor® Specimen Trap, 3.2-EPR-COL-O EndoRotor® 3.2mm Endoscopic Powered Resection (EPR) Catheter – Colonoscope Short Olympus, 3.2-EPR-COL-OP EndoRotor® 3.2mm Endoscopic Powered Resection (EPR) Catheter – Colonoscope Long Olympus/Pentax

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011697028%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011697028