FDA Device Establishments · JSON-LD · Markdown

Arthrex Australia Pty Ltd.

FEI 3019269298 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3019269298
Owner / OperatorARTHREX, INC. (#1220287)
AddressSuite 501, 20 Rodborough Road, Frenchs Forest New South Wales, 2086, AU
Mandatory US AgentArthrex Inc
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FSM
Regulation § (21 CFR)878.4800
Proprietary namesorthopedic manual instrument

External sources

Source: openFDA. Public-domain (CC0).