Philips receives FDA 510(k) clearance for next-generation reusable SpO₂ clip sensor

July 21, 2026New sensor advances pulse oximetry reliability for diverse patient populations through innovation and rigorous validation.Cambridge, ...
MobiHealthNews

FDA clears Masimo’s forehead sensor for pulse oximetry monitoring

Irvine, California-based Masimo Technologies, which makes non-invasive patient monitoring devices and sensors, has received FDA 510(k) clearance for its forehead sensor. The adhesive TFA-1 Forehead ...
Medscape

Class I Recall of GE Healthcare TruSignal SpO2 Sensors

GE HealthCare is recalling 7559 TruSignal arterial oxygen saturation (SpO2) sensors because of problems that may reduce defibrillation energy, expose patients to unintended voltage, or give inaccurate ...
Business Wire

Masimo Announces FDA Clearance of the Rad-G™ Pulse Oximeter

IRVINE, Calif.--(BUSINESS WIRE)--Masimo (NASDAQ: MASI) announced today FDA clearance of the Rad-G™ Pulse Oximeter, a rugged handheld device that provides clinically proven SET ® pulse oximetry, ...
CSR Wire

Medtronic Study of Investigational Nellcor™ Pulse Oximetry Technology Demonstrates Positive Results Across a Full Range of Skin Tones

January 22, 2026 /3BL/ – Medtronic, a global leader in healthcare technology, announced verification study results for its investigational Nellcor™ pulse oximetry with Nell-EQ™ intelligent processor ...
Wellbeing Magazine on MSN

Patient monitoring devices in general practice: A practical guide for GP clinics

Accurate patient monitoring is not an optional extra in general practice. It is a fundamental part of the clinical encounter, informing diagnosis, guiding treatment decisions and flagging ...