Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013687630

FEI Number

3013687630

Entity Name

MELOQ AB

City/State/Country

Stockholm, SE

Establishment Address

Brannkyrkagatan 72, Stockholm 118 23, SE

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Meloq AB (Owner Number: 10056849)

Owner / Operator Contact Address

Brannkyrkagatan 72, Stockholm, SE-AB 118 23, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KHX	Platform, Force-Measuring	Physical Medicine	Class 1	890.1575	2025-02-13
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2018-01-22

Official Correspondent

No official correspondent registered.

US Agent Details

Jane Campbell Business: J & D CAMPBELL ASSOCIATES, INC. Email: jdcainc.sc@gmail.com Phone: (843) 3143670

Related Public Records

Same Entity

Meloq 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 3013687630. Last updated year: 2026. Please use registration number 3013687630 when referencing this establishment in official correspondence.