Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005504113

FEI Number

3005504113

Entity Name

KEMENTEC SOLUTIONS AS

City/State/Country

Taastrup Hovedstaden, DK

Establishment Address

Kuldyssen 10, Taastrup Hovedstaden 2630, DK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kementec Solutions A/S (Owner Number: 10042694)

Owner / Operator Contact Address

Kuldyssen 10, Taastrup, DK-84 2630, DK

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
PPM	General Purpose Reagent	Pathology	Class 1	864.4010	2012-12-19

Official Correspondent

No official correspondent registered.

US Agent Details

Dan Keefe Business: Kementec Solutions Inc. Email: contact@kementec.com Phone: (617) 3367474

Related Public Records

Same Entity

Kementec Solutions A/S

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 3005504113. Last updated year: 2026. Please use registration number 3005504113 when referencing this establishment in official correspondence.