Circadia Health, Inc.

FDA Device Registration & Listing · El Segundo, CA, US · Registration 3017812398

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
3017812398
FEI Number
3017812398
Entity Name
Circadia Health, Inc.
City/State/Country
El Segundo, CA, US
Establishment Address
507 S Douglas St, El Segundo, CA 90245, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Circadia Technologies (Owner Number: 10078542)
Owner / Operator Contact Address
Runway East Borough Market, 20 St Thomas Street, London, GB-ENG SE1 9RS, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

The Circadia C100 System The Circadia C200 System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2020-11-05
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2024-07-16
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) Cardiovascular Class 2 870.2300 2024-07-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Circadia Technologies
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
K913749 Edentec Corp. EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 1992-07-02
K771407 Research Development Corp. LUNG VOLUME & PRESSURE MONITOR 1977-08-04
K122223 Philips Medizin Systeme Boeblingen GmbH NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO 2013-04-12
K832250 Litton Medical Electronics SERVOMED BASIC BEDSIDE UNIT SMA 102- 1984-06-01
K801515 Abbott Medical Electronics Co. ABBY II PATIENT MONITOR OR VITAL SIGNS M 1980-07-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017812398. Last updated year: 2026. Please use registration number 3017812398 when referencing this establishment in official correspondence.
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