Neogen Culture Media

FDA Device Registration & Listing · LANSING, MI, US · Registration 1120041

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1120041
FEI Number
1120041
Entity Name
Neogen Culture Media
City/State/Country
LANSING, MI, US
Establishment Address
740 EAST SHIAWASSEE, LANSING, MI 48912, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NEOGEN CORP. (Owner Number: 9028759)
Owner / Operator Contact Address
620 LESHER PLACE, --, Lansing, MI 48912, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mueller Hinton Agar Cystine Lactose Electrolyte Deficient (CLED) Agar

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth Microbiology Class 2 866.1700 2007-11-16
JSH Culture Media, Non-Selective And Differential Microbiology Class 1 866.2320 1992-11-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NEOGEN CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812581 Uti-Tect, Inc. SENSI-TECT 1981-09-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1120041. Last updated year: 2026. Please use registration number 1120041 when referencing this establishment in official correspondence.
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