# ATEX CO., LTD.

FEI: 3014133483
Status: Active
Establishment types: Sterilize Medical Device for Another Party (Contract Sterilizer); Develop Specifications But Do Not Manufacture At This Facility; Remanufacture Medical Device; Reprocess Single-Use Device; Manufacture Medical Device for Another Party (Contract Manufacturer); Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device; Foreign Private Label Distributor; Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: ATEX Co., Ltd. (#10060111)

Address: 3-3-24 Nagayoshi-kawanabe, Hirano-ku, Osaka, 547-0014, JP

Mandatory US Agent: FIUS Distributors, LLC

## Products

Total registered: 1
Top product codes: ISA
Regulation §: 890.5660

Proprietary names: Lourdes; OHCO

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014133483%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014133483