FDA Device Entity Profile: KENT ELASTOMER PRODUCTS, INC.

Known Identifiers & Locations

FEI Numbers 3002303166, 3003502083, 3004995608

Owner Operator Numbers 9044738

Locations Covered Dundee, OH, US; KENT, OH, US; MOGADORE, OH, US

Registered Establishments (3)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
3002303166	KENT ELASTOMER PRODUCTS, INC.	KENT, OH, US	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3003502083	KENT ELASTOMER PRODUCTS, INC.	Dundee, OH, US	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details
3004995608	KENT ELASTOMER PRODUCTS, INC	MOGADORE, OH, US	Manufacture Medical Device for Another Party (Contract Manufacturer)	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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