KENT ELASTOMER PRODUCTS, INC

FDA Device Registration & Listing · MOGADORE, OH, US · Registration 3004995608

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
3004995608
FEI Number
3004995608
Entity Name
KENT ELASTOMER PRODUCTS, INC
City/State/Country
MOGADORE, OH, US
Establishment Address
3890 MOGADORE INDUSTRIAL PRKWY, MOGADORE, OH 44260, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
KENT ELASTOMER PRODUCTS, INC. (Owner Number: 9044738)
Owner / Operator Contact Address
1500 ST. CLAIR AVE., --, Kent, OH 44240, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FREE-BAND

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2005-01-27

Official Correspondent

Brian Lipowski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KENT ELASTOMER PRODUCTS, 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
3003502083 KENT ELASTOMER PRODUCTS, INC. Dundee, OH, US
3002303166 KENT ELASTOMER PRODUCTS, INC. KENT, OH, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004995608. Last updated year: 2026. Please use registration number 3004995608 when referencing this establishment in official correspondence.
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