ACTIM OY

FDA Device Registration & Listing · Espoo Uusimaa, FI · Registration 1000212994

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
1000212994
FEI Number
1000212994
Entity Name
ACTIM OY
City/State/Country
Espoo Uusimaa, FI
Establishment Address
Klovinpellontie 3, Espoo Uusimaa FI-02180, 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
3013143953 Actim Oy Manufacturing Site Joensuu Pohjois-Karjala, FI

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000212994. Last updated year: 2026. Please use registration number 1000212994 when referencing this establishment in official correspondence.
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