Fulgent Genetics, Inc. (NASDAQ: FLGT) ("Fulgent," or the "Company"), a technology-based company with a well-established ...

GUILFORD, Conn., November 07, 2024--Hyperfine, Inc. announces CE approval of its latest generation of AI-powered Swoop® system software under the European Medical Device Regulation.

Femasys receives CE mark certification for FemBloc System, the first non-surgical permanent birth control solution approved in Europe.

CE-certification | Regulatory Newsgenedrive plc ("genedrive" or the "Company") Genedrive® CYP2C19 ID Kit receives CE-certification under the European In Vitro Diagnostics Regulation genedrive plc ...

On the 20th, global medical aesthetic specialist CLASSYS announced that it has obtained European CE Medical Device Regulation (MDR) certification for its monopolar radiofrequency (MRF) device ...

MatOrtho’s ReCerf hip resurfacing arthroplasty (HRA) has secured the CE mark, signifying its adherence to European safety standards.

"EpiMonitor's availability in Europe is a great milestone for the epilepsy community," said Simone Tognetti, Empatica's CTO Co-founder. "Our goal is to continue bringing technology that improves ...

It appears that OnePlus is preparing to launch its Nord 5 series of smartphones soon. The reason behind this is that the Nord CE 5 has received approval from the UAE’s TDRA certification ...

Dr. Carlos Ciller, CEO and co-founder of RetinAI, commented: “Receiving CE-MDR certification for LuxIA underscores our shared commitment with FVS to advance leading-edge ophthalmic care to ...

Business Wire Empatica Achieves CE MDR Certification for EpiMonitor, Bringing Round-the-Clock Epilepsy Monitoring to Europe 28 May 2025 BOSTON ...