Meet longitudinal clinical-grade heart monitoring designed for the bra women already wear.
Heart disease is the leading cause of death in women, yet screening often starts too late. Baseline cardiovascular screening should begin at or before age 45, during the critical perimenopause transition when intervention is most effective.
Models shaping future care are trained on incomplete data missing women, obscuring sex-specific risk and treatment response. We are building the missing piece.
Only 1 in 1,000 clinical trials focus on menopause.
60% of women will have a cardiovascular disease by 2050 (AHA, 2026)
0 major foundation models trained on hormonal or cycle data.
The inframammary position is the most information-rich location in the body for continuous cardiovascular and hormonal monitoring. It's the foundation of everything Braave measures.
A direct window into cycle-driven dynamics that shape cardiovascular risk.
Bypasses subcutaneous fat for a cleaner signal and lower noise floor.
The inframammary fold sits directly above the cardiac apex, closer than any other wearable.
Seamless by design, the Underfit is a clinical-grade biosensing interface capturing 45+ sex-specific cardiovascular biomarkers from the inframammary fold, where the undercurve of the breast meets the chest wall.
A continuous, longitudinal dataset of women's cardiovascular and hormonal signals. Data is opt-in, de-identified, HIPAA-aligned, GDPR-ready. Built to fill the gap most health AI was trained without. Open to academic, clinical, pharma, and AI lab partnerships.
research@wearebraave.co →Most wearables rely on optical sensors to estimate heart rate. The Underfit™ captures the heart's direct electrical activity from the chest, alongside core temperature precise to a tenth of a degree. This medical-grade ECG tracking reveals micro-signals that shift in tandem with hormones.
Braave is a continuous monitoring system, not a diagnostic device. Lab-validated against clinical-grade ECG with the University of Portsmouth and FDA-grade core temperature. Pursuing Class II 510(k) clearance.
What it is: The corrected interval between heart-muscle depolarization and repolarization.
Why it matters: Even small extensions can signal hormonal shifts, and elevated cardiac risk in women that PPG sensors miss entirely.
What it is: The time it takes for the atria to depolarize.
Why it matters: Estrogen modulates atrial conduction; subtle changes here track ovulation, perimenopause, and stress with remarkable precision.
What it is: Beat-to-beat fluctuation in the segment between ventricular depolarization and repolarization.
Why it matters: Hormonal cycles, autonomic state, and recovery all leave fingerprints here.
What it is: Microvolt-level alternations in the T-wave's shape.
Why it matters: A subclinical signal that's been linked to estrogen withdrawal, anxiety load, and elevated arrhythmia risk in female physiology.
What it is: The duration of ventricular depolarization — the electrical pulse that triggers each heartbeat.
Why it matters: Estrogen influences ventricular conduction speed; subtle QRS widening has been associated with perimenopause, elevated cardiovascular risk, and autonomic dysregulation in women.
What it is: A continuous electrical reading at ±1–2 ms timing accuracy, validated against gold-standard hospital ECG.
Why it matters: Most consumer wearables read 30-second snapshots; clinical-grade means we never stop listening.
Braave provides continuous clinical-grade patient reported data measured outside of appointments and labs, integrated with the tools you already use.
Current tools collect fragmented signals: steps, sleep, snapshots, hormone tests. Braave is the layer that's been missing.