FDA Device Establishments · JSON-LD · Markdown

Planmeca Oy

FEI 1000207287 · Manufacture Medical Device · Status: Active

FEI Number1000207287
Owner / OperatorPlanmeca Oy (#10023612)
AddressAsentajankatu 6, Helsinki Uusimaa, 00880, FI
Mandatory US AgentPlanmeca U.S.A. Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NOF
Regulation § (21 CFR)872.3661
Proprietary namesPlanmeca Emerald S; Planmeca Emerald

External sources

Source: openFDA. Public-domain (CC0).