Focused on the future of breast regeneration.

BellaSeno is advancing a bioresorbable scaffold platform designed to guide soft tissue formation at scale. Starting with breast applications, this approach supports the body’s own processes to generate, integrate, and adapt tissue over time.

Clinical Trial
Progressed
Greater Than
26
patients
LONGEST FOLLOW-UP
up to 3 years
Target
106
patients
Inside the Scaffold

Leading the regenerative platform with over 19 Patents

Treatment Focus

Revision & Restoration

Addressing silicone explant patients and soft-tissue defects through scaffold-guided restoration.

Primary Augmentation

Provide temporary soft-tissue support designed to guide natural volume restoration over time.

Breast Reconstruction

Supporting soft-tissue restoration after mastectomy or lumpectomy through scaffold-guided natural regeneration over time.

Designed for a Better Outcome*

Volume
Creation

Provides volume and shape while supporting the formation of the patient's own tissue.

Porous
Architecture

Highly interconnected pores facilitate cell infiltration, vascularization, and tissue in-growth.

Gradual
Resorption

Engineered to resorb predictably over time, leaving behind viable, regenerated tissue.

Tissue
Integration

Supports seamless integration with surrounding tissue for natural-feeling outcomes.

For Surgeons

Familiar Surgical Workflow

Designed for seamless integration into established surgical techniques.

Soft-Tissue
Support

Designed to provide temporary soft-tissue support of the patient’s own tissue.

Strategic Patient Opportunity

A differentiated approach to unmet market needs in revision and post weight-loss procedures.

Future Data
Generation

Built to generate long-term evidence on safety and effectiveness.

BRV-004 Trial Results 

Trial
Completed

Successfully completed clinical feasibility evaluation.

19 Patient
Cohort

Clinical study conducted across a 19-patient cohort.

2-Year Results Completed

Validated outcomes assessed through two-year follow-up.

83% Volume
Retention

Demonstrated sustained soft-tissue volume retention over time.

Study Program

Early Feasibility

Prospective feasibility studies and initial safety evaluation.

Ongoing Evidence Generation

Longitudinal follow-up and data maturation across indications.

CE Mark

Enabling future scalability across global markets.