Actim Oy Manufacturing Site

FDA Device Registration & Listing · Joensuu Pohjois-Karjala, FI · Registration 3013143953

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013143953
FEI Number
3013143953
Entity Name
Actim Oy Manufacturing Site
City/State/Country
Joensuu Pohjois-Karjala, FI
Establishment Address
Noljakantie 13,, ,, Joensuu Pohjois-Karjala FI-80130, FI
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Actim Oy (Owner Number: 10048029)
Owner / Operator Contact Address
Klovinpellontie 3, Espoo, FI-18 FI-02180, FI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K123986
PMA Number
N/A

All Registered Proprietary Names

Actim PROM Actim PROM Controls

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OAM Immunoassay, Insulin-Like Growth Factor Binding Protein-1 Clinical Chemistry Class 1 862.1550 2014-11-28

Official Correspondent

No official correspondent registered.

US Agent Details

Jamie Harris Business: Icon Clinical Research Email: jamie.harris@iconplc.com Phone: (661) 6459048

Related Public Records

Same Entity

Actim Oy
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1000212994 ACTIM OY Espoo Uusimaa, FI

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013143953. Last updated year: 2026. Please use registration number 3013143953 when referencing this establishment in official correspondence.
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