NeuraNova receives FDA 510(k) clearance for STEDI Device
Milestone establishes the first FDA-cleared product in NeuraNova’s portable neurotechnology portfolio LOS ANGELES–(BUSINESS WIRE)–NeuraNova, Inc., a medical technology company developing portable, noninvasive technologies for neurological care, today announced that the U.S. Food and Drug Administration has granted 510(k) clearance to... Read More →
TYBR Health announces $30 million series A financing to expand access to the B3 GEL® System
HOUSTON, July 21, 2026 /PRNewswire/ — TYBR Health today announced a $30 million Series A financing led by Vensana Capital and Mutual Capital Partners, with participation from Neovate Capital Partners and existing investors. The company will use the funds to... Read More →
Psychiatry lacks biomarkers. Can this EEG ballcap get a base hit? Featuring Universal Brain
Universal Brain just announced an FDA 510(k) clearance for its Neurotique™ platform, which offers a five-minute assessment to measure cognitive and emotional brain function in support of psychiatric diagnosis and treatment. The device is an eight-channel dry EEG baseball cap... Read More →
Approximately NIS 70 million investment in national infrastructure for AI models based on biological data featuring TeraCyte Analytics
New Israel BioToken Factory Initiative (IBFI) Brings Together NVIDIA, Teva, Sheba Medical Center, Startups and Universities to Develop the Next Generation of Biological AI The Israel Innovation Authority today announced a NIS 70 million investment, together with leading industry partners,... Read More →
ClearCam™ Selected by AFWERX for SBIR Phase I Award to Advance ClearScope IQ™ Surgical Visualization Technology
Austin-based medtech company awarded $74,360 to explore AI-enabled surgical visualization technology for Department of the Air Force applications AUSTIN, Texas, July 9, 2026 /PRNewswire/ — ClearCam™, Inc., an Austin-based medical device company focused on minimally invasive surgery, announces it has... Read More →
First successful human cases using first console-free portable Cryocatheter system for bronchoscopic procedures featuring Endocision
Initial Cases Follow FDA Clearance in the U.S. and Health Canada Approval MONTREAL (July 7, 2026) — Endocision is pleased to announce the successful completion of the first series of human clinical cases using its Cryocision flexible cryocatheter system at... Read More →
Neuspera Integrated Sacral Neuromodulation System (iSNM) to Receive Same Medicare Payment as Legacy Implantable SNM Devices Under Proposed 2027 CMS Rule
Reimbursement Parity Advances Patient Access and Will Help More Patients Avoid the Pain, Complications, and Repeat Surgeries Common in the $1 Billion Legacy Sacral Neuromodulation (SNM) Market Served by Boston Scientific and Medtronic SAN JOSE, Calif., July 8, 2026 /PRNewswire/... Read More →
Winter Innovations Receives FDA 510(k) Clearance and PCCP Authorization for Expanded EasyWhip® Family
Knoxville, TN – Winter Innovations, Inc. a medical device company developing innovative solutions for orthopedic soft tissue surgery, announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the expanded EasyWhip® Family. The EasyWhip® Family... Read More →
Abcam Antibodies Validated for CUT&RUN featuring EpiCypher
Abcam and EpiCypher have partnered to set a higher standard for antibody validation in CUT&RUN. By uniting Abcam’s deep recombinant antibody expertise with EpiCypher’s advanced chromatin profiling innovation, this collaboration delivers robust CUT&RUN antibodies validated to meet the demands of... Read More →
Pain monitoring data to be available in hospital EHRs through Philips Capsule featuring Medasense Biometrics
he integration enables streaming of the patient’s NOL-Nociception Level Index® data to EHRs, supporting personalized analgesia in surgery and critical care. US, ISRAEL, July 7, 2026 /EINPresswire.com/ — Objective pain-monitoring data obtained via Medasense’s PMD-200™ patient monitor and its NOL-Nociception... Read More →