The range
Medical devices
One platform, certified for a defined purpose and built on Regenerative Intelligence™. This page carries the regulatory framing that the aesthetic range does not need.
Who this range is for
Clinics and practitioners operating within a medical scope: doctors, nurses and allied health professionals, and clinic owners whose setting is registered accordingly. If your premises operate under a local authority special treatment licence rather than a medical registration, the aesthetic range is the starting point.
HEBE
Regenerative Intelligence™: a regenerative platform with four energy delivery technologies, designed to reactivate the body’s own regenerative capacity in a controlled and precise way. Full details, applicators and clinical integration on the HEBE page.
Certification and intended purpose
HEBE is CE-marked as a medical device, certified through notified body 1639 and manufactured under ISO 13485 and ISO 9001. Its certified intended purpose covers musculoskeletal, rheumatic and pelvic floor applications. Aesthetic use falls outside that scope and is described on this site as such.
UK market status — MHRA registration and UK Responsible Person — is being confirmed and will be published here.
Training and support
Practitioner training is delivered by our clinical team and covers modes, parameters, contraindications and protocols. See Training and certification.
Arrange a demonstration
In your clinic, with the UK team.
