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FDA 510(k)

Noxturnal Web

K-Number: K260585 · 2026-03-20

Decision Date2026-03-20
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Noxturnal Web is the device name listed in this FDA 510(k) record. The listed applicant is Nox Medical Ehf. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K260585. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Noxturnal Web?

Noxturnal Web is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Nox Medical Ehf. The 510(k) number is K260585.

When did Noxturnal Web receive FDA 510(k) clearance?

Noxturnal Web received FDA 510(k) clearance on 2026-03-20, under 510(k) number K260585.

Who is the listed applicant for Noxturnal Web?

The FDA 510(k) record lists Nox Medical Ehf as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Noxturnal Web?

The FDA product code for Noxturnal Web is OLV.

Other records listing Nox Medical Ehf as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: OLV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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