# KANEKA AMERICAS HOLDING INC

FEI: 3014758755
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: KANEKA AMERICAS HOLDING INC (#10095053)

Address: 7979 Gateway Blvd, Newark, CA, US



## Products

Total registered: 2
Top product codes: KRA, QJP
Regulation §: 870.1210, 870.1250

Proprietary names: Surfrider 13 Microcatheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014758755%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014758755