MedtechSourcebook

KENT ELASTOMER PRODUCTS, INC.

Contract manufacturer ยท Kent, OH

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2005Product codes first listed, by year (tallest: 1)2026
FDA registration
3002303166 (openFDA record; or search FDA's registration database)
FEI number
3002303166
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
KENT ELASTOMER PRODUCTS, INC. (FDA owner/operator no. 9044738)
Registered address
1500 Saint Clair Ave, Kent, OH 44240
Contract listings
2 device listings, 2 product codes, first listed Sep 20, 2005
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
GBWCatheter, PeritonealClass IGeneral and plastic surgeryContract manufacturingSep 20, 2005
PUIDrape, Surgical, ExemptClass IIGeneral and plastic surgeryContract manufacturingJan 16, 2023

Other contract facilities of KENT ELASTOMER PRODUCTS, INC.