# NEMOTO KYORINDO CO., LTD.

FEI: 3008918179
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: NEMOTO KYORINDO CO., LTD. (#9043772)

Address: 2-12-23 Aoki, Kawaguchi Plant, KAWAGUCHI-SHI Saitama, 332-0031, JP

Mandatory US Agent: NEMOTO MEDICAL U.S., INC.

## Products

Total registered: 1
Top product codes: DXT
Regulation §: 870.1650

Proprietary names: PRESS DUO elite AG, PRESS DUO elite

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008918179%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008918179