Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007905163

FEI Number

3007905163

Entity Name

TRIONIC SVERIGE AB

City/State/Country

Uppsala, SE

Establishment Address

Marstagatan 8, Uppsala SE-753 23, SE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Trionic Sverige AB (Owner Number: 10031941)

Owner / Operator Contact Address

Marstagatan 8, Uppsala, SE-AB SE-753 23, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Trionic

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITJ	Walker, Mechanical	Physical Medicine	Class 1	890.3825	2010-03-23

Official Correspondent

Johan Kuikka

US Agent Details

Oshin Mahmodi Business: TRIONIC USA INC Email: info@trionic.us Phone: (818) 4801907

Related Public Records

Same Entity

Trionic Sverige AB

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011958210	KUNSHAN LANDON TRADE CO. LTD	Kunshan Jiangsu, CN

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3039346864	FIRST NATION GROUP, LLC	Niceville, FL, US
3029740428	ORA MEDICAL INC	Montreal Quebec, CA
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007905163. Last updated year: 2026. Please use registration number 3007905163 when referencing this establishment in official correspondence.