The Market Online - At The Bell

Join our daily newsletter At The Bell to receive exclusive market insights

  • Sleep-tech company Oventus has received U.S. FDA approval for its sleep apnoea device, O2Vent Optima
  • The approval allows the company to begin selling its product in the U.S. market and launch pre-established supply agreements
  • Shares in Oventus are up 11.46 per cent today, currently trading for $0.54 apiece

Sleep-tech company Oventus has received U.S. FDA approval for its sleep apnoea device, O2Vent Optima.

Getting the all clear from The States’ food and drug regulatory body, this allows the company to begin sales in the U.S. market.

Prior to the O2Vent being cleared by the U.S. federal agency, Oventus established supply agreements with American-based sleep groups, which can now officially launch.

CEO of Oventus Dr Chris Hart said: “We look forward to officially launching our material agreements within US sleep channels and working with our customers across their various treatment sites to deliver Optima devices to patients.”

After achieving regulatory approvals in the U.S., Oventus expects it will fast track its expansion across the The States, Canada and Australia. Over the next 12-24 months, the company is working to secure several supply agreements.

The O2Vent Optima is a custom, 3D-printed nylon oral appliance, resembling a mouthguard in appearance. It is designed to help patients with obstructive sleep apnoea by enabling unobstructed air to flow to the back of the throat.

Multiple clinical studies have proven this technology to be effective with more than 170 patients benefiting from it.

The company highlighted going forward it is secure in scaling sales significantly, due to $9.3 million raised from shareholders earlier in the year.

Shares in Oventus are up 11.46 per cent today, currently trading for $0.54 apiece, as of AEST 11:32 am.

OVN by the numbers
More From The Market Online

ResMed spikes on robust results and global growth spurt

ResMed shares have climbed following the release of the company's strong Third Quarter FY2024 results.

PharmAust CEO’s sayanora triggers stock plunge

Clinical-stage biotechnology company, PharmAust shares plunged 24 per cent so this morning, following the resignation of…

Recce wins safety board approval to dose 4g in R327 UTI infusion trial

Recce Pharma will dose patients with 4g of its R327 intravenous solution to treat UTIs in…

Emyria locks in $2.3M to progress MDMA research – with Chair adding $0.3M

WA-based and ASX-listed Emyria is seeking to further research using MDMA to treat PTSD. The chair…