FDA grants breakthrough designation for Blue Arbor’s RESTORE System
The RESTORE System can connect to a patient’s residual muscles and peripheral nerves, surpassing skin electrode technologies.
25 April 2024
25 April 2024
The RESTORE System can connect to a patient’s residual muscles and peripheral nerves, surpassing skin electrode technologies.
The Auto-Pure 2400 liquid handling platform is designed for ease of use and provides efficient workflows in the lab.
GlobalData estimates that 625,000 new brain tumour cases are diagnosed annually worldwide, with 70,000 of those cases in the US.
The restructuring includes the appointment of Steve Sandweg as the new CEO, as well as a new board of directors.
The company will use the funds to submit its extravascular temporary pacing lead system to the FDA.
Pelvital’s Flyte device is approved by the US FDA to treat stress urinary incontinence (SUI) and weakened pelvic floor muscles.
Speakers emphasised the need for classification and approval of devices, and effective licencing and quality control at BioTrinity 2024.
Curio’s MamaLift Plus is an eight-week prescription digital therapeutic that provides symptomatic relief for postpartum depression.
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