NightWare Receives the US FDA’s Approval for the First Medical Device to Stop NightMAres Related to PTSD

 NightWare Receives the US FDA’s Approval for the First Medical Device to Stop NightMAres Related to PTSD

NightWare Receives the US FDA’s Approval for the First Medical Device to Stop NightMAres Related to PTSD

Shots:

  • The US FDA has permitted marketing of a device intended for the temporary reduction of sleep disturbance related to nightmares in patients aged ≥22 yrs. suffering from nightmare disorder or PTSD
  • Nightware utilizes Apple Watch and an iPhone that is configured and logged into a software application and the Nightware server and monitors the wearer’s HR and movement while they sleep and if they are having a nightmare, gently arouse them out of the dream without waking up completely, using the smartwatch’s vibrations
  • The platform received the US FDA’s BT designation in May’2019 and now is available by prescription only and is intended for home use

Click here ­to­ read full press release/ article | Ref: FDA | Image: IT PRO

Tuba Khan

Tuba Khan is Senior Editor at PharmaShots. She is curious, creative, and passionate about recent updates and innovation in the Life sciences industry. She covers Biopharma, MedTech, and Digital health segments. Tuba also has an experience of digital and social media marketing and runs the campaigns independently. She can be contacted on tuba@pharmashots.com

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