Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006158025

FEI Number

3006158025

Entity Name

Lonza Verviers SRL.

City/State/Country

Verviers Liege, BE

Establishment Address

Parc Industriel de Petit-Rechain, Verviers Liege BE-4800, BE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

LONZA WALKERSVILLE, INC. (Owner Number: 9098883)

Owner / Operator Contact Address

8830 BIGGS FORD RD, --, Walkersville, MD 21793, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Culture Media Supplement

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JCF	Lymphocyte Separation Medium	Hematology	Class 1	864.8500	2018-04-30
IBG	Trypsin	Pathology	Class 1	864.4400	2018-05-02
JSK	Supplement, Culture Media	Microbiology	Class 1	866.2450	2019-02-25
PPM	General Purpose Reagent	Pathology	Class 1	864.4010	2018-04-30

Official Correspondent

Khushboo Mistry

US Agent Details

Khushboo Mistry Business: LONZA WALKERSVILLE, INC. Email: khushboo.mistry@lonza.com Phone: (301) 8987025

Related Public Records

Same Entity

LONZA WALKERSVILLE, INC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1114298	LONZA WALKERSVILLE, INC.	WALKERSVILLE, MD, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006158025. Last updated year: 2026. Please use registration number 3006158025 when referencing this establishment in official correspondence.