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O2Vent T

OVENTUS MANUFACTURING PTY LTD · Model O2Vent T · UDI-DI 09351567000011

LRK Prescription
1
510(k) clearances
2,783
Adverse events (1 deaths)
10
Recalls
108
Facilities

Description

The O2Vent T is a removable medical device that is fitted in the patient’s mouth and is intended to reduce or alleviate snoring and mild to moderate obstructive sleep apnea (OSA). The O2Vent T is made up of three parts: 1. The Upper Tray fitted over the upper teeth, with the breathing port at the front leading to the airways on each side to the rear of the appliance, is made from medical grade titanium 2. The Lower Tray fitted over the lower teeth, positions the jaw for mandibular advancement. The Upper and Lower Trays have a "landing area” customized to the patientsteeth and made from medical grade polymers. 3. The Upper and Lower Trays are connected together with a connector. A hook mechanism attached to the Upper Tray fits into a socket attached to the Lower Tray and positions the lower jaw forward, preventing the soft tissue of the throat from collapsing and obstructing the airway. An Adjustment Key for the O2Vent T allows the patient and their Clinician to adjust the protrusion of the lower jaw to the most effective and comfortable position.

Recalls

DateFirmReason
2026-04-27Prismatik Dentalcraft, Inc.Due to device not having FDA Clearance
2025-10-09Myofunctional Research Company USADue to firm mistakenly distributing product within the U.S. without FDA premarket clearance/approval.
2022-05-23Dental Choice Holding LlcThe device was marketed and sold in the US without FDA clearance.
2017-09-01Respire MedicalPotential for device breakage during use
2017-09-01Respire MedicalPotential for device breakage during use
2017-09-01Respire MedicalPotential for device breakage during use
2017-09-01Respire MedicalPotential for device breakage during use
2017-09-01Respire MedicalPotential for device breakage during use
2009-07-27Medtronic Xomed, Inc.Medtronic Xomed, Inc. is recalling the Repose Bone Screw System product and Bone Screw product due to improper labeling. The labeling for the Repose System was inadvertently place
2009-07-27Medtronic Xomed, Inc.Medtronic Xomed, Inc. is recalling the Repose Bone Screw System product and Bone Screw product due to improper labeling. The labeling for the Repose System was inadvertently placed

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.