Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030979160

FEI Number

3030979160

Entity Name

INTERLINKED AB

City/State/Country

Stockholm, SE

Establishment Address

Regeringsgatan 82, Stockholm 11139, SE

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Interlinked AB (Owner Number: 10090480)

Owner / Operator Contact Address

Regeringsgatan 82, Stockholm, SE-AB 11139, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LinkUS Drain

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBX	Catheter, Irrigation	General, Plastic Surgery	Class 1	878.4200	2024-04-03

Official Correspondent

Rebecca Bejhed

US Agent Details

Mindy McCann Business: Qserve Group US Inc. Email: USagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Interlinked AB

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 3030979160. Last updated year: 2026. Please use registration number 3030979160 when referencing this establishment in official correspondence.