# NIHON KOHDEN AMERICA, INC.

FEI: 2080783
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: NIHON KOHDEN CORP. (#8030227)

Address: 15353 Barranca Pkwy, Irvine, CA, US



## Products

Total registered: 2
Top product codes: GWQ, OLV
Regulation §: 882.1400

Proprietary names: TL-220T, TG-921T3, TL-052S, TL-201T, JE-921A, TL-062S

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%222080783%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=2080783