Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002497578

FEI Number

3002497578

Entity Name

KNUDSEN PLAST A/S

City/State/Country

Frederiksvaerk Hovedstaden, DK

Establishment Address

Industrivej 21, Frederiksvaerk Hovedstaden 3300, DK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Knudsen plast A/S (Owner Number: 10084813)

Owner / Operator Contact Address

Industrivej 21, Frederiksvaerk, DK-84 3300, DK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EmbryoSlide

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQK	Labware, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6160	2022-04-04

Official Correspondent

Lene Thygesen

US Agent Details

Marissa Vilchez Business: MDSS Email: mvilchez@mdss.com Phone: (312) 9751694

Related Public Records

Same Entity

Knudsen plast 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 3002497578. Last updated year: 2026. Please use registration number 3002497578 when referencing this establishment in official correspondence.