FDA Clears Steerable Biopsy Needles

Serpex Medical seeks to use steerable instruments to enable greater precision and access to improve the diagnosis and treatment of lung cancer.

Serpex Logo
Serpex

Serpex Medical announced U.S. FDA 510(k) clearance of its Compass Steerable Needles – steerable biopsy needles that enable precise access to lung nodules in the intrapulmonary region. Serpex Medical seeks to use steerable instruments to enable greater precision and access to improve the diagnosis and treatment of lung cancer. The clearance of the Compass Steerable Needles follows the recent clearance of Serpex's Recon Steerable Sheath.

"Precision is essential for confidence in diagnosing lung cancer, especially out in the lung periphery," says Sasha Schrode, President and Chief Executive Officer of Serpex Medical. "We are excited to deliver another innovative product that empowers clinicians to more successfully diagnose lung cancer at an earlier stage."

"This is another significant milestone in the team's pursuit of practical, intuitive innovation," says Duke Rohlen, Executive Chairman of Serpex Medical and Chief Executive Officer of Ajax Health & Zeus Health. "Now with two sets of clearances, Serpex is poised to make a significant impact on the standard of care for patients with lung cancer."

Serpex Medical is backed by Ajax Health, Zeus Health, Aperture Venture Partners and Western Technology Investment.

More in Surgical