REMOTE TECHNOLOGIES, INC.

FDA Device Registration & Listing · Port Chester, NY, US · Registration 1222777

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
1222777
FEI Number
1000120772
Entity Name
REMOTE TECHNOLOGIES, INC.
City/State/Country
Port Chester, NY, US
Establishment Address
10 Midland Ave Ste 207, Port Chester, NY 10573, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
REMOTE TECHNOLOGIES, INC. (Owner Number: 9003294)
Owner / Operator Contact Address
PO Box 1185, --, Greenwich, CT 06836, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K912323
PMA Number
N/A

All Registered Proprietary Names

TechSwitch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZL System, X-Ray, Mobile Radiology Class 2 892.1720 2007-12-10

Official Correspondent

CHERYL MAKRINOS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

REMOTE 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
K153059 Minxray, Inc. HF1202H PowerPlus Portable X-ray Equipment 2016-02-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-1470-2023 FUJIFILM Healthcare Americas Corporation 2
FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams
Z-3158-2024 FUJIFILM Healthcare Americas Corporation 2
The device is a mobile x-ray system designed to work with Fujifilm's GOS and CsI scintillator FDR D-EVO2 (DR-ID) 12XXSE) family of digital x-ray detectors coupled.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1222777. Last updated year: 2026. Please use registration number 1222777 when referencing this establishment in official correspondence.
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