FDA Device Establishments · JSON-LD · Markdown

KINJO RUBBER CO., LTD.

FEI 3015746529 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3015746529
Owner / OperatorKinjo Rubber Co., Ltd. (#10094387)
Address4-25, 1-Chome, Atobe-Kitanocho, Yao-City Osaka, 581-0068, JP
Mandatory US AgentFUJIFILM Healthcare Americas Corporation
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)FDF, FDS
Regulation § (21 CFR)876.1500
Proprietary namesDH-126STL; DH-116STL; DH-106STL; DH-096ST

External sources

Source: openFDA. Public-domain (CC0).