Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1834244

FEI Number

1000220700

Entity Name

GRANDRAPIDS FOAM TECHNOLOGIES, INC.

City/State/Country

Grand Rapids, MI, US

Establishment Address

1700 Alpine Ave NW, Grand Rapids, MI 49504, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

GRAND RAPIDS FOAM TECHNOLOGIES, INC. (Owner Number: 9007959)

Owner / Operator Contact Address

1700 Alpine Avenue NW, --, Grand Rapids, MI 49504, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Styrker suction ring without tubing Styrker suction mat (low profile) stryker suction mat (comfort) Stryker Suction ring with tubing, IsoFlex LAL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GCX	Apparatus, Suction, Operating-Room, Wall Vacuum Powered	General Hospital	Class 2	880.6740	2013-05-02
IOQ	Bed, Flotation Therapy, Powered	Physical Medicine	Class 2	890.5170	2018-09-04

Official Correspondent

Mike Amann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GRAND RAPIDS FOAM TECHNOLOGIES, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K890935	Dermanetics Corp.	SYSTEM 3000 FLUIDIZED AIR BED	1989-03-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1834244. Last updated year: 2026. Please use registration number 1834244 when referencing this establishment in official correspondence.