MedtechSourcebook

ROGERS FOAM CORPORATION

Contract manufacturer ยท Mt Sterling, KY

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

2003Product codes first listed, by year (tallest: 2)2026
FDA registration
3004082002 (openFDA record; or search FDA's registration database)
FEI number
3004082002
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
ROGERS FOAM CORPORATION (FDA owner/operator no. 1216617)
Registered address
310-A Flint Drive, Mt Sterling, KY 40353
Contract listings
5 device listings, 5 product codes, first listed Apr 10, 2003
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
CCXSupport, Patient PositionClass IAnesthesiologyContract manufacturingSep 15, 2009
FMWCover, Mattress (Medical Purposes)Class IGeneral hospitalContract manufacturingMar 24, 2008
FNMMattress, Air Flotation, Alternating PressureClass IIGeneral hospitalContract manufacturingMar 24, 2008
IKYMattress, Flotation Therapy, Non-PoweredClass IGeneral hospitalContract manufacturingNov 30, 2022
LRPTray, SurgicalClass IGeneral and plastic surgeryContract manufacturingApr 10, 2003

Other contract facilities of ROGERS FOAM CORPORATION