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The FENIX® Continence Restoration System:
Restore control, regain confidence

On April 27, 2017 Torax Medical announced the discontinuation of sales and clinical studies of the FENIX® Continence Restoration System. This is solely a business decision based on fit with Torax and Ethicon's strategic business plans and is not due to any safety concerns with the FENIX system.

Clinical support for physicians and implanted patients is unaffected by this decision. The FENIX device does not require any adjustment or maintenance.

If you have had a FENIX system implanted and have any questions or concerns regarding your implant, please contact your physician directly.

Humanitarian Device: Authorized by the Federal (USA) Law for use in the treatment of fecal incontinence in patients who are not candidates for or have previously failed conservative treatment and less invasive therapy options (e.g., injectable bulking agents, radiofrequency ablation, sacral nerve stimulation). The effectiveness of this device for this use has not been demonstrated.