About Beakn

Devices that read your body.
And tell you what it means.

Beakn makes smart health devices and the AI that connects them. A ring, a band, a scale, glasses, and clinical monitors — all feeding a single picture of how you actually are, updated continuously, explained in plain English.

What we believe
01

Signal over noise.

Every metric we surface is one worth acting on. We remove dashboards. We surface what changed and why.

02

Your data stays yours.

Your health data is stored in India and never sold or shared with advertisers. You can delete everything, permanently, at any time.

03

Earn the alert.

Beakn doesn't ping you. The devices have no screen, no buzz. The app speaks only when it has something worth saying.

04

Clinically validated hardware.

The ECG and blood pressure modules are FDA-cleared through our hardware partner. We build on sensors that have been independently tested — not just benchmarked in a lab we run.

05

Wellness, not medicine.

Beakn is a wellness product. We are honest about what the data means and when you should see a doctor instead of trusting an app.

Hardware credentials

Built on sensors that
have been independently tested.

The ECG, blood pressure, and oximetry modules in Beakn devices are manufactured by a certified medical device partner with multiple FDA clearances and peer-reviewed validation. These are the credentials that back those sensors.

FDA 510(k) — ECG Module
The ECG sensor hardware inside Beakn clinical monitors holds FDA 510(k) clearance for single-lead ECG recording and rhythm detection in adults.
ECG Device
FDA 510(k) — Blood Pressure + ECG Monitor
The BP+ECG hardware carries a separate FDA 510(k) clearance for oscillometric blood pressure measurement with simultaneous single-lead ECG capture.
BP + ECG Device
FDA 510(k) — Pulse Oximeter
The SpO₂ sensor hardware holds FDA 510(k) clearance for wrist-worn blood oxygen saturation and pulse rate monitoring.
Oximeter
Oxford University · JMIR 2022
An independent peer-reviewed study published in the Journal of Medical Internet Research validated the SpO₂ sensor hardware against controlled hypoxia from 100% down to 80% SaO₂. Results met ISO 80601-2-61:2019 accuracy requirements (RMSE <4%).
Published Study
ISO 13485 — Manufacturing
The clinical sensor hardware is manufactured in an ISO 13485-certified facility — the international quality management standard for medical device design, production, and post-market surveillance.
Quality Standard

FDA clearances verified via FDA 510(k) database · Oxford study: Santos M et al., JMIR 2022, PMID 35166690