Boppli
Commercial- Indications
- Neonatal critical care blood pressure monitoring
Company intelligence / Profile preview
Boppli®, the company’s lead product, received FDA Breakthrough Device Designation and FDA 510(k) clearance in September 2023. It provides continuous, non-invasive blood pressure monitoring for critically ill infants as an alternative to invasive arterial lines or intermittent cuff-based measurements. Clinical studies have demonstrated its value in NICU settings. Adult and home-use products are under development.
2 more assets in the full pipeline.
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