This section introduces the focused ultrasound systems used in fibroid treatment from a technical perspective. The method itself — how it works, who may be a candidate, its limits — is covered in our HIFU section; this is the device and technology layer.
Ultrasound-guided HIFU (USgHIFU)
The systems described on this site are ultrasound-guided: targeting and monitoring are performed with real-time ultrasound imaging throughout the procedure. MR-guided focused ultrasound (MRgFUS) applies the same physical principle under MRI guidance and is a separate family of systems; the literature evaluates the two approaches separately.
Our systems
PRO2008
A focused ultrasound platform with a top-mounted dry treatment probe, C-arm structure and TPS treatment planning.
PRO300
Six-axis robotic movement, adaptive planning (aTPS) and a portable design; a Class IIb medical device carrying the CE 0197 mark.
Our documentation approach
Every technical statement about the devices is based on official manufacturer documentation and regulatory records, and sources are shown openly on each page. Certification demonstrates a device’s legal status — clinical outcome evidence is a separate matter, which we address at method level in our Evidence section.