Cloud DX Inc.

FDA Device Registration & Listing · Kitchener Ontario, CA · Registration 3010984687

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
3010984687
FEI Number
3010984687
Entity Name
Cloud DX Inc.
City/State/Country
Kitchener Ontario, CA
Establishment Address
100 - 72 Victoria Street S, Kitchener Ontario N2G 4Y9, CA
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
CloudDX Inc. (Owner Number: 10048345)
Owner / Operator Contact Address
20 Jay St, Suite 834, Brooklyn, NY 11201, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K172795
PMA Number
N/A

All Registered Proprietary Names

Cloud DX JPD-FR412 Dual Mode Thermometer (Forehead and Ear)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FLL Continuous Measurement Thermometer General Hospital Class 2 880.2910 2021-12-20

Official Correspondent

No official correspondent registered.

US Agent Details

FDAIMPORTS.COM FDAIMPORTS.COM Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

CloudDX 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
K010462 Avita Corporation AVITA PICCOLO/EXATO INFARED EAR THERMOMETER (TS2 & TS4 SERIES) 2001-04-11
K760421 Arbrook Mfg. Corp. THERMOMETER, SURVALENT-ELECTRONIC 1976-08-23
K813409 Yellow Springs Instrument Co., Inc. MODEL 2100 DUAL-DISPLAY TELE-THERMOMETER 1981-12-18
K830039 Science Development Corp. SDC RECTAL TEMP. PROBE PRODUCT #1020 1983-02-23
K842199 Sharp Electronics Corp. ELEC. DIGITAL THERMOMETER MT-20 & 30 1984-07-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010984687. Last updated year: 2026. Please use registration number 3010984687 when referencing this establishment in official correspondence.
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