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Nox Medical

Iceland IS-MF-000000950 Last updated 23 Oct 2026

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Devices
110
Registries
EUDAMEDFDA 510(k)GUDIDFDA
FDA recalls
1

Catalogue110

Page 1 of 3

Showing 1-50 of 110

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2021

    • 7 Sep 2021 Z-0031-2022 Class II Terminated Error in the device firmware results in the inaccurate detection of device position.

What Nox Medical makes

Nox Medical manufactures respiratory monitoring devices including the Nox T3s System, Nox A1S SAS kit, T3s Recorder, and various RIP belts in different sizes, along with accessories like snap-on leads and body cables.

The company's products are classified as Class I, Class II, and Class IIa medical devices and are listed in the EU's EUDAMED and FDA's 510(k) databases. Nox Medical is based in Iceland.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Nox Medical manufacture?

Nox Medical manufactures respiratory monitoring devices including the Nox T3s System, Nox A1S SAS kit, T3s Recorder, and various RIP belts in different sizes, along with accessories like snap-on leads and body cables.

Where is Nox Medical based?

Nox Medical is based in Iceland, as indicated by the country code IS in the device data.

Which regulatory registries list Nox Medical's devices?

Nox Medical's devices are listed in the EU's EUDAMED database and the FDA's 510(k) database, as specified in the device data.

How are Nox Medical's devices classified?

Nox Medical's devices are classified as Class I, Class II, and Class IIa medical devices, which indicates varying levels of regulatory control based on their potential risk to patients.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Iceland
Address
2, Katrinartun, Reykjavik, Iceland
Phone
+354 5707170
EUDAMED SRN
IS-MF-000000950
FDA FEI number
3007389703