In the news
30
Sep

2025

Resitu Medical Receives 510(k) Marketing Authorization from US FDA for its Breast Biopsy Device

Resitu Medical has received FDA 510(k) authorization for the RESL09 breast cancer biopsy device. This handheld minimally invasive device excises tissue samples with diameters up to 9 mm and will first reach market in the US. The company plans to expand the tool’s clinical claims and core size range.

Resitu breast tissue biopsy device, RESL09
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