{"id":104605,"date":"2026-02-06T21:48:06","date_gmt":"2026-02-06T21:48:06","guid":{"rendered":"https:\/\/pakistaninewspaperlist.com\/news\/hemex-health-receives-fda-breakthrough-device-designation-for-gazelle-hb-variant-test\/"},"modified":"2026-02-06T21:48:06","modified_gmt":"2026-02-06T21:48:06","slug":"hemex-health-receives-fda-breakthrough-device-designation-for-gazelle-hb-variant-test","status":"publish","type":"post","link":"https:\/\/pakistaninewspaperlist.com\/news\/hemex-health-receives-fda-breakthrough-device-designation-for-gazelle-hb-variant-test\/","title":{"rendered":"Hemex Health Receives FDA Breakthrough Device Designation for Gazelle\u00ae Hb Variant Test"},"content":{"rendered":"<div id=\"main-body-container\" itemprop=\"articleBody\">\n<p>PORTLAND, Ore., Feb.  06, 2026  (GLOBE NEWSWIRE) &#8212; Hemex Health, a medical diagnostics company focused on decentralized testing for blood-based conditions, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation to its Gazelle\u00ae Hb Variant Test.<\/p>\n<p>The FDA\u2019s Breakthrough Devices Program is intended to expedite the development, assessment, and review of medical devices that have the potential to provide more effective diagnosis or treatment of life-threatening or irreversibly debilitating diseases. Through the program, Hemex will receive prioritized interaction and feedback from the FDA as it advances development of the Gazelle Hb Variant Test.<\/p>\n<p>\u201cThe Breakthrough Device Designation reflects the FDA\u2019s recognition of the need for improved tools to support the management of sickle cell disease,\u201d said Patti White, CEO of Hemex Health. \u201cWe appreciate the opportunity for early and frequent engagement with the agency as we continue to develop diagnostic technologies intended to deliver clinically meaningful information closer to patients.\u201d<\/p>\n<p>The Gazelle\u00ae platform is designed to rapidly separate and detect hemoglobin fractions and variants using miniaturized electrophoresis technology, with the goal of enabling decentralized access to quantitative hemoglobin data. Hemex is exploring the potential role of this technology in supporting therapeutic monitoring and disease management in sickle cell disease and other hemoglobinopathies.<\/p>\n<p>Hemex recently presented multiple scientific posters and an oral presentation related to sickle cell disease diagnostics and monitoring at the 66th American Society of Hematology (ASH) Annual Meeting, reflecting ongoing research and clinical engagement around hemoglobin variant testing.<\/p>\n<p>The Gazelle Hb Variant Test has not been cleared or approved by the FDA and is not available for sale in the United States. Breakthrough Device Designation does not guarantee regulatory clearance.<\/p>\n<p><strong>About Hemex Health<\/strong><br \/>Hemex Health impacts health outcomes in the world\u2019s most challenging markets by developing affordable point-of-care diagnostics that quickly deliver clinically actionable diagnostic solutions for blood-based conditions. The company\u2019s diagnostic solutions are affordable for both low- and high-income areas and simple enough to be used by anyone.\u00a0<\/p>\n<p>Gazelle technology was developed in collaboration with Case Western Reserve University. Hemex Health is in Portland, Oregon, U.S.A, and Mumbai and Coimbatore, India. More information can be found at\u00a0<a href=\"https:\/\/www.globenewswire.com\/Tracker?data=TukMuoc2SuQ3lchvq5P2TeRIWA1mabkD1_5D8bZjGvYdCf81PbnaCkeNCfTQNukYjk3ThnR1cfrmO2T0MOdckv5aT1lW64kGIHqPfNbK9wPsS9NqcyWGwhXQFEjgxbtGMPiXB2dXOrg73OvJOsXciiCaJ0kMOSUa2IMxOGFmjL7qjsn1-YDsDb9kLcAQ_F5WfCKRzHYIE5deNbz5G8yVS51dezxyi5JtUUYN-qHMOMXu8Qu4TfBtU5Y6T1mJ8Zu3X6IWMl1FWmpm4t9tF5aM4chQM5MjiwrX4y2fOpg_w8hNNZFroD1D3xr9MaJPD4gl2kC77_cTaXzOtfM8gpA145pzvFMmuPXj41IKGmQpmPvey602PmKD5Ar1HQThJhO9uLkm5fKS1rw7oIqZHEEFu68NqP05E-3GxPgHNgoTEJ3YGgERJGE37uxZw0VHuMjviitoDF1HAK79meCPvd4H2X_gmMFUbmeEQ1_GSZNAanUrP7ZkvTqu-e741ugHLrGU42wlHL6reghT-VMQXwMLNECtKD_8X-GRAl8tyFpTHzsq2KMRCGwsUMwDMLaKMbzZRkeKsk8510wI06JQTltINA==\" rel=\"nofollow\" target=\"_blank\" title=\"www.hemexhealth.com\">www.hemexhealth.com<\/a>.<\/p>\n<p>MEDIA CONTACT:<\/p>\n<p>Judi Sakowski<\/p>\n<p>j.sakowski@hemexhealth.com<\/p>\n<p>+1 503-754-2377<\/p>\n<p>\n            <\/div>\n","protected":false},"excerpt":{"rendered":"<p>PORTLAND, Ore., Feb. 06, 2026 (GLOBE NEWSWIRE) &#8212; Hemex Health, a medical diagnostics company focused on decentralized testing for blood-based conditions, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation to its Gazelle\u00ae Hb Variant Test. The FDA\u2019s Breakthrough Devices Program is intended to expedite the development, assessment, and [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":104606,"comment_status":"","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"fifu_image_url":"https:\/\/ml.globenewswire.com\/Resource\/Download\/ce43760e-7a02-4094-99cb-128b0d0c6449","fifu_image_alt":"","footnotes":""},"categories":[208],"tags":[],"class_list":["post-104605","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-globenewswire"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO 4.9.8 - aioseo.com -->\n\t<meta name=\"description\" content=\"PORTLAND, Ore., Feb. 06, 2026 (GLOBE NEWSWIRE) -- Hemex Health, a medical diagnostics company focused on decentralized testing for blood-based conditions, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation to its Gazelle\u00ae Hb Variant Test. 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