Nox A1 System

Catalogue number NOX-A1PSG_USF, listed by Nox Medical Ehf, IS, under Automatic Event Detection Software For Polysomnograph With Electroencephalograph. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OLZ
Manufacturer City Province Registered as Device types
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13

Record

Regulatory record for Nox A1 System
Listed by Nox Medical Ehf, IS
FDA product code OLZ
Device type Automatic Event Detection Software For Polysomnograph With Electroencephalograph
Device class Class 2
Regulation 21 CFR 882.1400
510(k) K192469
Record published 2020-02-24
Record revised 2020-10-26 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Nox A1 System
Catalogue number Size Status
NOX-A1PSG_USF In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sleepware Respironics Inc. 8
Sleep Profiler Advanced Brain Monitoring, Inc. 3
EnsoSleep Ensodata, Inc. 3
Waveband Beacon Biosignals, Inc. 2
Nox A1® EEG 5 Lead Gold Electrode Cable Nox Medical Ehf 2
Nox A1® EEG Head Cable Nox Medical Ehf 2
Nox C1 Kit Nox Medical Ehf 2
Nox C1 Access Point Nox Medical Ehf 2
DeepRESP Nox Medical Ehf 1
Polysmith Version 12.0 Neurotronics, LLC 1
Nox A1s Recorder Nox Medical Ehf 1
Sphinx HB710 Head Box Neurotronics, LLC 1

Showing 12 of 31. All products under Automatic Event Detection Software For Polysomnograph With Electroencephalograph

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252330 2025-11-17
K241960 2025-03-14

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer