FDA Device Establishments · JSON-LD · Markdown

ZUIKO MEDICAL CORPORATION

FEI 3012441818 · Manufacture Medical Device · Status: Active

FEI Number3012441818
Owner / OperatorZuiko Medical Corporation (#10050258)
Address3-50 Torikaikami 4-chome, Settsu-city Osaka, 566-0062, JP
Mandatory US AgentZuiko Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KGX
Regulation § (21 CFR)880.5240
Proprietary namesPlus moist K; Plus moist SA-K

External sources

Source: openFDA. Public-domain (CC0).