RADIOLOGICAL IMAGING TECHNOLOGY, INC.

FDA Device Registration & Listing · Co Spgs, CO, US · Registration 1722661

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
1722661
FEI Number
1000160359
Entity Name
RADIOLOGICAL IMAGING TECHNOLOGY, INC.
City/State/Country
Co Spgs, CO, US
Establishment Address
5065 List Drive, Co Spgs, CO 80919, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RADIOLOGICAL IMAGING TECHNOLOGY, INC. (Owner Number: 9009383)
Owner / Operator Contact Address
5065 List Drive, --, Colorado Springs, CO 80919, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

RIT Family of Products RITg142 RITg135 RIT Classic RIT Film RIT Isocenter Analysis Tool RIT Complete RITg148 RIT113 Classic RIT Complete Diagnostic RITg142CK Radia Therapy RITg148+ RIT EPID MLC with Isocenter RIT EPID MLC Radia Diagnostic RIT113 FILM DOSIMETRY SYSTEM RIT113 RADIATION THERAPY DOSIMETRY

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IYE Accelerator, Linear, Medical Radiology Class 2 892.5050 1994-02-01

Official Correspondent

DANIEL RITT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RADIOLOGICAL IMAGING TECHNOLOGY, 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
K071992 Varian Medical Systems HIGH-DEFINITION 120 MULTILEAF COLLIMATOR (HD120 MLC) 2007-08-15
K253962 Radformation, Inc. ClearCheck (RADCC V2.7) 2026-04-03
K003779 Arplay Medical S.A. IMMOBILIZATION SYSTEM FOR ENT 2001-07-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0004-2019 Varian Medical Systems 2
TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product Usage: The TrueBeam delivery systems are intended to provide radiotherapy and stereotactic radiosurgery for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.
Z-0005-2019 Varian Medical Systems 2
VitalBeam Radiotherapy Delivery System Version 2.5 Product Usage: The VitalBeam delivery systems are intended to provide precision radiotherapy and stereotactic radiosurgery for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.
Z-0020-2015 N/A 2
Proteus 235 Proton Therapy System for cancer treatment.
Z-0035-2012 Accuray Incorporated 2
CyberKnife Robotic Radiosurgery System, Synchrony Respiratory Tracking System (Standard Treatment Couch). Synchrony Respiratory Tracking System, a Radiation Therapy Device, Model Numbers: 026429, 028185. Product is manufactured and distributed by Accuray, Inc., Sunnyvale, CA
Z-0036-2012 Accuray Incorporated 2
CyberKnife Robotic Radiosurgery System, Synchrony Respiratory Tracking System (Robocouch Patient Positioning System), a Radiation Therapy Device. Model Numbers: 026430, 028186. Product is manufactured and distributed by Accuray, Inc., Sunnyvale, CA

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3007791541 Varian Medical Systems China Co., Ltd. Beijing, CN
1932738 MEDTEC LLC Orange City, IA, US
3007165183 ITV Medizintechnik GmbH Innsbruck Tirol, AT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1722661. Last updated year: 2026. Please use registration number 1722661 when referencing this establishment in official correspondence.
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