# INTERVENE INC

FEI: 3030481118
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: InterVene Inc (#10094226)

Address: 2684 Middlefield Rd Ste E, Redwood City, CA, US



## Products

Total registered: 2
Top product codes: QEW, KRA
Regulation §: 870.5150, 870.1210

Proprietary names: Recana Thrombectomy Catheter System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223030481118%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3030481118