Epitel
Epitel received 510(k) clearance for two remote monitoring offerings and Curio Digital Therapeutics received clearance for its postpartum prescription digital therapeutic.
The company’s Seer Home device allows for potential epilepsy diagnosis through at-home data collection.
The company will use the funding to support the commercial expansion of its product.
The company's REMI product is currently FDA cleared for in-hospital use, but Epitel plans to expand into ambulatory and in-home care.