June 2026 Nihon Kohden received U.S. FDA 510(k) clearance for its TG-980P CO₂ Sensor Kit, expanding its capnography portfolio with advanced gaseous-phase carbon dioxide monitoring for patient monitoring systems.
May 2026 Medtronic (Covidien) received U.S. FDA 510(k) clearance for the Capnostream™ 35 Portable Respiratory Monitor, strengthening its portable capnography and respiratory monitoring portfolio for hospital and procedural care settings.
June 2025 Philips expanded its long-standing partnership with Medtronic through a new multi-year agreement to integrate Medtronic's Microstream™ capnography technology into Philips patient monitoring solutions, broadening access to advanced respiratory monitoring.