X-Nav Technologies, LLC announced that it has received 510(k) Clearance from the U.S. Food & Drug Administration for X-Mark™, a new virtual patient registration technology that advances navigated dental implant surgery. X-Mark enhances the company's industry-leading X-Guide® Dynamic 3D Navigation system to give dentists the ability to deliver more accurate dental implant procedures to more patients seeking new teeth. X-Mark features breakthrough technology to facil

Business Wire IndiaOtis eCall Customers call on Otis to support reopening strategies and facility-operation plans. Otis offers

LifeSignals Group, announced USFDA 510(k) clearance has been received for their LifeSignals ECG Remote Monitoring Patch Platform. The LifeSignals ECG Remote Monitoring Patch Platform is a wireless remote monitoring system intended for use by healthcare professionals for the continuous collection of Electrocardiography (ECG) and Heart Rate monitoring in ambulatory, hospital, home and healthcare settings. Data is transmitted wirelessly from the LifeSignals Wireless Medical Biosensor LP1250 to a

Patientco, a next-generation patient payment technology company, has signed an agreement with BJC HealthCare, one of the largest nonprofit healthcare organizations in the United States, to make it easier for BJC patients to navigate, understand and pay their medical expenses. As a leading health system with 15 hospitals and multiple community health locations, BJC sought an improved, more consistent financial experience for patients. Patientco will provide BJC with a seamless suite

Change Healthcare unveiled its nationwide Clinical Data Retrieval service, a new cloud-based interoperability solution that makes it possible for payers to quickly and easily retrieve patient records from the industry’s leading electronic health record (EHR) systems, and other EHRs. The service provides patient care data in an integrated, electronic fashion to verify claim accuracy, pay claims, manage risk profiles, improve plan designs, expand care coordination, satisfy quality reporti

FX received 510k clearances for their TiN (Titanium Nitride) Coated Humeral Heads and Glenospheres. The new addition of TiN coated humeral heads and glenospheres adds unique-to-market prostheses to the FX portfolio. The TiN coated humeral heads and glenospheres are identical to the current humeral heads and glenospheres that we offer but with the TiN coating applied. The TiN coated humeral head is compatible with the Humelock II and Humeris shoulder in the anatomic construct while t

BANNOCKBURN, Ill., July 20, 2020 (GLOBE NEWSWIRE) -- Option Care Health, Inc. (the “Company” or “Option Care Health”) (Nasdaq: OPCH), the nation’s largest independent provider of home and alternate site infusion services, announced today preliminary financial results for the second quarter ended June 30, 2020. Second Q

OXFORD, United Kingdom and MARLBOROUGH, Mass., July 20, 2020 (GLOBE NEWSWIRE) -- Oxford Immunotec Global PLC (Nasdaq:OXFD) (the "Company"), today announced that it has entered into a long-term agreement to supply its T-SPOT.TB test and associated accessories to the Stop TB Partnership - Global Drug Facility (GDF). This follows the inclusion of the T-SPOT.TB t

The Milken Institute Center for the Future of Aging announced today the launch of the Alliance to Improve Dementia Care. The Alliance will seek to transform and improve the complex health and long-term care systems that people at risk for and living with dementia must navigate. During the next 20 years, the Milken Institute projects that the number of Americans living with Alzheimer's disease or other dementias will nearly double to 13 million. Two-thirds of all people living wi

Empirical Spine, Inc., maker of the LimiFlex Paraspinous Tension Band, today announced completion of enrollment in its U.S. IDE trial studying the use of LimiFlex with a decompression for patients suffering from degenerative spondylolisthesis with lumbar spinal stenosis.  The trial compares outcomes of patients who receive either LimiFlex or transforaminal lumbar interbody fusion (TLIF) after decompression surgery.  The trial reached its target of 135 LimiFlex patients enrolled into