Tag: penumbra

Penumbra receives CE mark for Lightning Flash 2.0 and Lightning Bolt...

Penumbra today announced it has secured CE mark in Europe for two computer-assisted vacuum thrombectomy (CAVT) technologies—Lightning Flash 2.0 and Lightning Bolt 7.   “Based on...

Penumbra announces FDA clearance of Lightning Flash 2 for the treatment...

Penumbra has announced the US Food and Drug Administration (FDA) clearance and launch of Lightning Flash 2, the next generation computer assisted vacuum thrombectomy (CAVT)...

Venous News’ top stories of 2023

Which stories captured the attention of the venous community this year? Read our summary of the trending articles from across the Venous News network...

Penumbra expands computer-aided thrombectomy offering with Lightning Bolt 7 launch

Penumbra has announced the US Food and Drug Administration (FDA) clearance and launch of Lightning Bolt 7, which the company claims is the most...

Penumbra launches Lightning Flash mechanical thrombectomy system

Today, Penumbra announced the US Food and Drug Administration (FDA) clearance and launch of its Lightning Flash mechanical thrombectomy system. "Lightning Flash features Penumbra's novel...
Indigo

New data underscore benefits of Penumbra’s Indigo for submassive pulmonary embolisms...

In a new subgroup analysis of the EXTRACT-PE trial, the Indigo aspiration system (Penumbra) was effective at improving clinical outcomes for submassive pulmonary embolism...

Penumbra announces the European launch of the Indigo system with Lightning...

Penumbra has announced that its Indigo aspiration system with Lightning 7 and Lightning 12 have secured CE mark and are now commercially available in...
Indigo

Results published from EXTRACT-PE trial of Penumbra’s Indigo aspiration system

Results from the EXTRACT-PE trial, which found that Penumbra’s Indigo aspiration system met its predefined safety and efficacy endpoints for the treatment of pulmonary...

Penumbra’s newest generation of Indigo aspiration system receives FDA clearance for...

Penumbra today announced US Food and Drug Administration (FDA) 510(k) clearance for expanded indication of the latest iteration of the Indigo aspiration system, Lightning...