exGraft
Commercial- Indications
- Vascular disease
Company intelligence / Profile preview
PECA Labs has achieved over 1,000 human implants of its first device with excellent results. The MASA Valve received Humanitarian Use Device designation from the FDA and began an early feasibility study at five US sites in 2023. exGraft family of vascular grafts has expanded CE Mark approval for use in Europe. Clinical data show improved freedom from re-operation compared to current options for pediatric cardiac surgery
4 more assets in the full pipeline.
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