Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009307605

FEI Number

3009307605

Entity Name

LOJER OY

City/State/Country

Sastamala Pirkanmaa, FI

Establishment Address

Putajantie 42, Sastamala Pirkanmaa FIN-38210, FI

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lojer Oy (Owner Number: 10053833)

Owner / Operator Contact Address

Putajantie 42, Sastamala, FI-11 FIN-38210, FI

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Lojer Capre FX Treatment Table Lojer Manuthera 242 Lojer Capre M Treatment Table Lojer Capre F Treatment Table

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
INQ	Table, Powered	Physical Medicine	Class 1	890.3760	2017-01-16

Official Correspondent

No official correspondent registered.

US Agent Details

Sandra Hernandez Business: Scrip Companies Email: shernandez@scripco.com Phone: (630) 7717400

Related Public Records

Same Entity

Lojer Oy

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009307605. Last updated year: 2026. Please use registration number 3009307605 when referencing this establishment in official correspondence.