|Adaptive Biotechnologies Corp., of Seattle||Clonoseq assay||Diagnostic powered by immunosequencing||Detection and monitoring of minimal residual disease (MRD) in blood or bone marrow from patients with chronic lymphocytic leukemia||Received expanded U.S. FDA clearance; previously authorized for the detection and monitoring of MRD in patients with multiple myeloma and B-cell acute lymphoblastic leukemia using DNA from bone marrow samples|
|Cardiacsense Ltd., of Caesarea, Israel||Medical watch||Wristwatch with sensors for remote monitoring||For heart rate monitoring and detection of atrial fibrillation with ECG accuracy||Received the Israeli Ministry of Health's regulatory approval|
|Joimax, of Karlsruhe, Germany, and Irvine, Calif.||Intracs||Electromagnetic navigation tracking and control system||Allows for spinal procedures to be carried out with minimal X-ray control||Won U.S. FDA clearance|
|Scientia Vascular LLC, of Salt Lake City||Zoom Wire||Line of interventional guidewires||For gaining access during ischemic and hemorrhagic stroke and other challenging neurovascular and peripheral vascular procedures||Won U.S. FDA clearance|
|Surmodics Inc., of Eden Prairie, Minn.||Sublime Radial Access 0.014 Rapid Exchange (RX) percutaneous transluminal angioplasty dilatation catheter||250 cm working length; outer balloon diameters range from 2.0 mm to 4.0 mm with balloon lengths between 20 mm and 220 mm||Allows treatment of below-the-knee vessels from the radial arteries||Received 510(k) clearance from the U.S. FDA|
|Vela Diagnostics Pte. Ltd., of Singapore||Virokey SARS-CoV-2 RT-PCR Test||Probe-based, automated, reverse transcription PCR test||Detects SARS-CoV-2 in nasopharyngeal and oropharyngeal swabs||Received emergency use authorization from the U.S. FDA|
For more information about individual companies and/or products, see Cortellis.