# KINJO RUBBER CO., LTD.

FEI: 3015746529
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Kinjo Rubber Co., Ltd. (#10094387)

Address: 4-25, 1-Chome, Atobe-Kitanocho, Yao-City Osaka, 581-0068, JP

Mandatory US Agent: FUJIFILM Healthcare Americas Corporation

## Products

Total registered: 2
Top product codes: FDF, FDS
Regulation §: 876.1500

Proprietary names: DH-126STL, DH-116STL, DH-106STL, DH-096ST

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015746529%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015746529