Ventus Medical, Inc.

United States(FDA 510(k) applicant) Last updated 23 May 2026

Devices: 5
Registries: FDA 510(k)FDA
FDA recalls: 0

Catalogue5

Invent Snoring Device Ref K120665

Class I FDA 510(k) Active
Provent Professional Sleep Apnea Therapy (Provent 80); Provent Professional Sleep Apnea Therapy (Provent 50) Ref K102404

Class II FDA 510(k) Active
Provent Nasal Cannula Ref K080983

Class II FDA 510(k) Active
Provent Professional Sleep Apnea Therapy Ref K090398

Class II FDA 510(k) Active
Provent Nasal Dilator, Model BR2 Ref K071560

Class II FDA 510(k) Active

FDA establishments1

Registered with the FDA under this company group, matched by name.

Ventus Medical Limited GB

What Ventus Medical, Inc. makes

Ventus Medical, Inc. manufactures devices for treating sleep-related breathing disorders, including snoring and obstructive sleep apnea. Their portfolio includes nasal dilators, nasal cannulas, and oral snoring devices designed to improve airway patency during sleep. The company also produces professional-grade sleep apnea therapy systems with adjustable pressure settings.

The company’s devices are classified under FDA categories Class I and Class II, with relevant products listed via the 510(k) pathway. These products are regulated under U.S. medical device laws and are intended for use within the United States. No additional international registries are referenced in the device data.

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

Information

Country: United States(Country (from FDA 510(k) applicant address))

Catalogue5

Invent Snoring Device Ref K120665

Provent Professional Sleep Apnea Therapy (Provent 80); Provent Professional Sleep Apnea Therapy (Provent 50) Ref K102404

Provent Nasal Cannula Ref K080983

Provent Professional Sleep Apnea Therapy Ref K090398

Provent Nasal Dilator, Model BR2 Ref K071560

FDA establishments1

What Ventus Medical, Inc. makes

Information