GRI MEDICAL PRODUCTS, INC.

FDA Device Registration & Listing · CAVE CREEK, AZ, US · Registration 1222612

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1222612
FEI Number
1000120912
Entity Name
GRI MEDICAL PRODUCTS, INC.
City/State/Country
CAVE CREEK, AZ, US
Establishment Address
4937 E. RED RANGE WAY, CAVE CREEK, AZ 85331, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GRI MEDICAL PRODUCTS, INC. (Owner Number: 9000961)
Owner / Operator Contact Address
4937 E. RED RANGE WAY, --, Cave Creek, AZ 85331, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

INTUSSUSCEPTION AIR REDUCTION KIT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQT Evacuator, Gastro-Urology Gastroenterology, Urology Class 2 876.4370 2004-08-19

Official Correspondent

STEPHEN SNIDER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GRI MEDICAL PRODUCTS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1222612. Last updated year: 2026. Please use registration number 1222612 when referencing this establishment in official correspondence.
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