Notable regulatory approvals of emerging technologies over the past 30 days

Along with AI in its various iterations, the list may include virtual and augmented reality, 3D printing and visualization, robotics and other innovative technologies changing healthcare delivery.

Nanowear: FDA clearance for AI diagnostics and monitoring via wearable nanosensor platform (Sept. 28)

Wyss Center: CE mark certification for longitudinal, AI-preparatory brain visualization cloud software (Sept. 29)

Siemens: FDA clearance for photon-counting CT detectors. Hailed by the agency as “the first new major technological improvement for computed tomography imaging in nearly a decade” (Sept. 30)

IotaMotion: FDA de novo classification for robotic-assisted cochlear implant insertion system (Oct. 5)

Amber Implants: FDA breakthrough device designation for 3D-printed spinal implant system (Oct. 5)

SyncThink: FDA clearance for AI analysis of eye movement in mobile concussion diagnostics (Oct. 5)

DreaMed: Expanded FDA clearance for AI-guided insulin administration (Oct. 6)

Medtronic: CE mark certification for robotic-assisted surgery system (Oct. 11)

Delphinus: FDA premarket approval for 3D breast ultrasound tomography (Oct. 12)

Subtle Medical: Health Canada approval for AI enhancement of MRI and PET imaging (Oct. 13)

Cognetivity Neurosciences: FDA approval for AI-aided rapid dementia assessment (Oct. 20)

Panakeia: CE mark certification for AI breast cancer image analysis (Oct. 21)

Naviswiss: FDA clearance for digital hip replacement surgery planning (Oct. 21)

Dave Pearson

Dave P. has worked in journalism, marketing and public relations for more than 30 years, frequently concentrating on hospitals, healthcare technology and Catholic communications. He has also specialized in fundraising communications, ghostwriting for CEOs of local, national and global charities, nonprofits and foundations.

Around the web

The tirzepatide shortage that first began in 2022 has been resolved. Drug companies distributing compounded versions of the popular drug now have two to three more months to distribute their remaining supply.

The 24 members of the House Task Force on AI—12 reps from each party—have posted a 253-page report detailing their bipartisan vision for encouraging innovation while minimizing risks. 

Merck sent Hansoh Pharma, a Chinese biopharmaceutical company, an upfront payment of $112 million to license a new investigational GLP-1 receptor agonist. There could be many more payments to come if certain milestones are met.