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76-90 of 795 results
Apollo Endosurgery completes merger with San Diego-based Lpath
US medical devices company Apollo Endosurgery and therapeutic antibodies developer Lpath have completed the merger that was announced in September this year.
Patient Care > Patient Monitoring > News
AirXpanders gets FDA de novo clearance for AeroForm tissue expander system
By MDBR Staff Writer
Medical device firm AirXpanders has received de novo clearance from the US Food and Drug Administration (FDA) for its AeroForm tissue expander system.
Patient Care > Patient Monitoring > News
FDA approves Alcon’s new AcrySof multifocal toric intraocular lens
By MDBR Staff Writer
Novartis subsidiary Alcon has secured approval from the US Food and Drug Administration (FDA) for its AcrySof IQ ReSTOR +3.0D multifocal toric intraocular lens (IOL).
Patient Care > Patient Monitoring > News
First two patients implanted in EndoStim's LESS GERD clinical trial
HonorHealth Research Institute and EndoStim announced that the first two patients have been implanted with the EndoStim device in the Lower Esophageal Sphincter Stimulation for GERD (LESS GERD) trial.
Patient Care > Patient Monitoring > News
FDA approves Masimo’s TFA-1 single-patient-use forehead sensor
By MDBR Staff Writer
Masimo has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its TFA-1 single-patient-use adhesive forehead sensor.
Patient Care > Patient Monitoring > News
Aethlon Medical begins sepsis-related virus study
By MDBR Staff Writer
Aethlon Medical has started Sepsis-related virus study, focusing on cytomegalovirus, epstein-barr and herpes simplex viruses.
Patient Care > Patient Monitoring > News
ReadCoor receives grant to support novel pathogen detection system
ReadCoor announced a multi-year grant from the Bill & Melinda Gates Foundation to apply their proprietary spatial sequencing technology to understand causes of childhood mortality.
Patient Care > Patient Monitoring > News
ADM Tronics spearheads new initiative for medical therapy device to treat tinnitus
ADM Tronics announced that its subsidiary, Aurex International Corporation (AIC), will spearhead the launch of a re-engineered version of ADMT's patented, FDA-cleared, proprietary medical device Aurex-3.
Patient Care > Patient Monitoring > News
NeuroMetrix features Quell in Huffington’s new Thrive Global platform
NeuroMetrix announced that its Quell wearable pain relief technolog is featured in the new Thrive Global commerce platform.
Patient Care > Patient Monitoring > News
Nevro announces filing of lawsuit by Boston Scientific
Nevro, a global medical device company that is providing innovative evidence-based solutions for the treatment of chronic pain, announced that Boston Scientific has filed a lawsuit for patent infringement.
Patient Care > Patient Monitoring > News
ReSound launches new pediatric smart hearing aid in US
ReSound announced the US launch of ReSound Up Smart, the only pediatric Smart Hearing aid with Made for iPhone capabilities, providing new ways to support speech and language development, educational skills, and social interaction.
Patient Care > Patient Monitoring > News
Centurion Medical launches Compass digital pressure transducers
By MDBR Staff Writer
Centurion Medical Products has expanded its Compass platform with the introduction of new digital pressure transducers to measure and monitor pleural and intra-abdominal pressures (IAP).
Patient Care > Patient Monitoring > News
Mölnlycke Health Care, Rochal partner to introduce skin care products
By MDBR Staff Writer
Swedish medical solutions firm Mölnlycke Health Care has signed a licensing agreement with US biomedical R&D company Rochal Industries to strengthen prevention solutions offering.
Patient Care > Patient Monitoring > News
Sanovas introduces new and improved solution for endotracheal intubation
Life science asset holding firm Sanovas has launched its LightSpeed Intubation System (LSI), a new and improved solution for endotracheal intubation.
Patient Care > Patient Monitoring > News
Nanowear gets FDA approval for SimplECG remote diagnostic monitoring device
By MDBR Staff Writer
Nanowear has secured class II 510(k) clearance from the US Food and Drug Administration (FDA) for its SimplECG remote diagnostic monitoring device.
Patient Care > Patient Monitoring > News
76-90 of 795 results