Rachel Klemovitch, Assistant Editor06.03.24
This past month, new devices, device recalls, and AI capabilities were popular among readers.
The AltaValve and the transcatheter mitral valve replacement (TMVR) device from 4C Medical received the FDA’s Breakthrough Device designation.
Elekta launched a new high-definition artificial intelligence (AI)-enhanced imaging—Evo CT-Linac. CT-Linac uses powerful AI capabilities to deliver offline and online adaptive radiation therapy, as well as improved standard image-guided radiation therapy.
Medtronic recalled its SonarMed Airway Monitors due to reported issues with the device’s monitors and acoustic sensors. Hologic also issued a recall for its BioZorb Marker because of complications and events reported with implanted devices.
Trail data was released at Heart Rhythm 2024 that showed how AI can provide an individualized non-invasive approach to determine targets of ablation in persistent AF.
The AltaValve and the transcatheter mitral valve replacement (TMVR) device from 4C Medical received the FDA’s Breakthrough Device designation.
Elekta launched a new high-definition artificial intelligence (AI)-enhanced imaging—Evo CT-Linac. CT-Linac uses powerful AI capabilities to deliver offline and online adaptive radiation therapy, as well as improved standard image-guided radiation therapy.
Medtronic recalled its SonarMed Airway Monitors due to reported issues with the device’s monitors and acoustic sensors. Hologic also issued a recall for its BioZorb Marker because of complications and events reported with implanted devices.
Trail data was released at Heart Rhythm 2024 that showed how AI can provide an individualized non-invasive approach to determine targets of ablation in persistent AF.
- Heart Rhythm 2024: AI-Guided Afib Treatment Better Than Standard Therapy
- Partner Preference in Full-Service Medical Device Outsourcing
- 4C Medical Gets 2 FDA Breakthough Nods for AltaValve TMVR Device
- ESTRO24: Elekta Releases Evo AI-Powered, Adaptive CT-Linac
- Pulse Biosciences Names Burke Barrett as President & CEO
- Medtronic Recalls SonarMed Airway Monitors After Injury
- From CMO to CDMO: Breaking Down the M&A Level-Up
- Defining the Future of Quality and Regulatory Operations in Medtech
- Hologic Has a Serious Recall of the BioZorb Marker
- What Happened to the Reprocessing of Single-Use Devices?—ThrowbackThursday