# KENT ELASTOMER PRODUCTS, INC.

FEI: 3003502083
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: KENT ELASTOMER PRODUCTS, INC. (#9044738)

Address: 7369 PEABODY-KENT RD., Dundee, OH, US



## Products

Total registered: 1
Top product codes: GBW
Regulation §: 878.4200

Proprietary names: K 600 LATEX TUBING, Penrose Drain Non-Sterile, KEP NON-STERILE, THERMOPLASTIC TUBING, KEP NON STERILE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003502083%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003502083