|Alveo Technologies Inc., of Alameda, Calif.||Be.well COVID-19 Flex Test||Point-of-care molecular test based on an isothermal nucleic acid amplification process||Detects SARS-CoV-2||Received the CE mark|
|Cardiacsense Ltd., of Caesarea, Israel||Medical watch||Wearable that integrates sensors and software algorithms to provides continuous patient monitoring||Detects of atrial fibrillation and monitors heart rate variability with continuous photoplethysmography and spot electrocardiogram||Received the CE mark|
|Kantaro Biosciences LLC, of New York||COVID-Seroklir||Semi-quantitative SARS-CoV-2 IgG antibody test kit; 2-step enzyme-linked immunosorbent assay (ELISA)||Detects the presence and precise level of SARS-CoV-2 IgG antibodies||The U.S. FDA has revised emergency use authorization to allow use in detecting high titer COVID-19 convalescent plasma|
|Surgical Planning Associates Inc., of Boston||Hipinsight||Augmented reality intra-operative guidance system||Guides surgeon during total hip arthroplasty||Received 510(k) clearance from the U.S. FDA|
|Visby Medical Inc., of San Jose, Calif.||Visby Medical COVID-19||Single-use polymerase chain reaction (PCR) device||For the qualitative detection of SARS-CoV-2||The U.S. FDA expanded emergency use authorization to allow for use at the point of care in CLIA-waived settings|
For more information about individual companies and/or products, see Cortellis.