DENVER, Nov. 06, 2024 (GLOBE NEWSWIRE) -- SeaStar Medical Holding Corporation (Nasdaq: ICU), a commercial-stage medical device company developing proprietary solutions to reduce the consequences ...

Medtech company DermaSensor has claimed FDA approval for a handheld device, powered by artificial intelligence (AI), that can be used to detect skin cancer at the point of care. The eponymous ...

SAE Media Group's 15th Annual Pre-Filled Syringes and Injectable Drug Devices Conference 2023 will be bigger than ever, with a pre-conference focus day exploring the advances in PFS design for ...

Revenue in the Drug Delivery Devices market market in Asia is anticipated to attain US$6.88bn in 2024. The revenue is forecasted to exhibit an annual growth rate (CAGR 2024-2029) of 6.16% ...

Nov 7 (Reuters) - The U.S. Food & Drug Administration has approved Johnson & Johnson's (JNJ.N), opens new tab device for a type of condition which causes abnormal heart rhythm, the company said on ...

The FDA has been evaluating AI-enabled medical devices for nearly 30 years with the FDA’s first approval of a partially AI-enabled device coming in 1995, when the FDA approved PAPNET ...

The US Food and Drug Administration announced a proposal to remove oral phenylephrine – a common ingredient in many popular over-the-counter decongestants – from the market, citing evidence ...

"iPad1,1": iPad "iPad2,1", "iPad2,2", "iPad2,3", "iPad2,4": iPad 2 "iPad3,1", "iPad3,2", "iPad3,3": iPad 3 "iPad3,4", "iPad3,5", "iPad3,6": iPad 4 "iPad6,11", "iPad6 ...

The FDA's Center for Devices and Radiological Health announced a pilot program designed to improve the timeliness of communications regarding high-risk medical device recalls. The initiative aims ...

How can drug delivery devices manage competing priorities – reducing overall carbon footprint without expense to patient and practitioner safety or treatment efficacy. Sustainability strategies must ...