OXYRASE, INC.

FDA Device Registration & Listing · MANSFIELD, OH, US · Registration 1530248

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
1530248
FEI Number
3000206015
Entity Name
OXYRASE, INC.
City/State/Country
MANSFIELD, OH, US
Establishment Address
3000 Park Avenue West, MANSFIELD, OH 44906, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OXYRASE, INC. (Owner Number: 9024787)
Owner / Operator Contact Address
3000 Park Avenue West, --, Mansfield, OH 44906, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kanamycin, Vancomycin, Laked Blood Agar Plate Brucella Blood Agar Plate Schaedler Blood Agar OxyPlate

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JSJ Culture Media, Selective And Non-Differential Microbiology Class 1 866.2360 1996-02-27
KZI Culture Media, Enriched Microbiology Class 1 866.2330 2001-05-12
JSG Culture Media, Non-Selective And Non-Differential Microbiology Class 1 866.2300 1996-02-27

Official Correspondent

Troy Menssen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OXYRASE, INC.
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
K863524 Bd Becton Dickinson Vacutainer Systems Preanalytic REGAN-LOWE CHARCOAL AGAR 1986-09-19
K880142 Hardy Media TSA W/LEC. & TWEEN. 80 1988-03-30

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0024-05 Remel, Inc. 1
Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1530248. Last updated year: 2026. Please use registration number 1530248 when referencing this establishment in official correspondence.
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