FDA Device Establishments · JSON-LD · Markdown

Arthrex Japan G.K. (Shinjuku)

FEI 3012470322 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3012470322
Owner / OperatorARTHREX, INC. (#1220287)
AddressShinjuku NS BLDG 28F, 2-4-1 Nishi-Shinjuku, Shinjuku-ku Tokyo, 1630828, JP
Mandatory US AgentARTHREX, INC.
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)HRS, HWC
Regulation § (21 CFR)888.3030, 888.3040
Proprietary namesArthrex Fracture Plates and Screws; Single/multiple component metallic bone fixation appliances and accessories

External sources

Source: openFDA. Public-domain (CC0).