MedtechSourcebook

GRANDRAPIDS FOAM TECHNOLOGIES, INC.

Contract manufacturer ยท Grand Rapids, MI

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

1994Product codes first listed, by year (tallest: 1)2026
FDA registration
1834244 (openFDA record; or search FDA's registration database)
FEI number
1000220700
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
GRAND RAPIDS FOAM TECHNOLOGIES, INC. (FDA owner/operator no. 9007959)
Registered address
1700 Alpine Ave NW, Grand Rapids, MI 49504
Contract listings
3 device listings, 3 product codes, first listed Jan 13, 1994
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
GCXApparatus, Suction, Operating-Room, Wall Vacuum PoweredClass IIGeneral hospitalContract manufacturingMay 2, 2013
IKYMattress, Flotation Therapy, Non-PoweredClass IGeneral hospitalContract manufacturingJan 13, 1994
IOQBed, Flotation Therapy, PoweredClass IIPhysical medicineContract manufacturingSep 4, 2018