FDA expands clearance for Inquis Medical’s Aventus thrombectomy system

Inquis Medical announced today that the FDA granted expanded 510(k) clearance for its Aventus thrombectomy system.

The expanded clearance means Aventus now has an indication to treat pulmonary embolism (PE). It comes around a month after the Menlo Park, California-based company shared positive study data for Aventus in PE. The study successfully met its primary endpoints, demonstrating safety and efficacy in treating acute intermediate-risk PE patients.

Aventus, a next-generation mechanical thrombectomy platform, features proprietary tissue-sensing technology. It provides operators with real-time information on the tissue composition in contact with the device. The system offers enhanced precision and control during procedures.

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