Company Transitions from Infrastructure Buildout to Active Market Execution as Expanded 510(k) Review Enters Final ...
1d
Diabeloop receives FDA 510(k) clearance for DBLG2, an Automated Insulin Delivery algorithm in an App
Diabeloop receives FDA 510(k) clearance for DBLG2, an Automated Insulin Delivery algorithm in an App: a strategic ...
HeartBeam (NASDAQ: BEAT) was among the medical device companies highlighted in a Jan. 8 report by Modern Healthcare by Lauren ...
The Naox Link system uses soft, biocompatible in-ear electrodes integrated into wired earbuds to acquire, record, and ...
MedPage Today on MSN
First in-ear EEG device gets FDA clearance
The Naox Link in-ear EEG platform is the first of its kind to be cleared for prescription use at home or in healthcare ...
Moving Biotech (4MB), a clinical stage biotechnology company developing next-generation, disease-modifying therapies for osteoarthritis (OA), today announced that the U.S. Food and Drug Administration ...
A2 Biotherapeutics, Inc. (A2 Bio), a clinical-stage cell therapy company developing first-in-class logic-gated cell therapies ...
Ceribell received breakthrough device designation for its LVO stroke detection monitor, and Naox Technologies secured 510(k) clearance for its in-ear EEG device.
This new FDA-cleared system uses modern follicle-stimulating technology and precision delivery methods to help reactivate ...
BrainSpace announced that the FDA granted 510(k) clearance for its Intellidrop automated brain fluid management system.
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