eSteth vs Keikku

eSteth is a world class digital stethoscope, designed to provide high quality heart & lung sounds to physicians & nurses for better diagnosis. eSteth also provides state-of-the-art support for Telemedicine. eSteth Lite is the affordable model. designed to support care providers in primary care and hospital settings while eSteth Pro is designed to work in professional healthcare settings to improve sound quality for diagnosis and live teleconsultations.

Keikku is an AI Clinical Platform designed to support clinicians throughout the patient encounter. Rather than switching between multiple disconnected tools, Keikku brings documentation, clinical reference, and AI-powered workflows together in one connected platform. Features • AI Scribe - Generate structured clinical documentation while you focus on your patient. • Clinical Reference - Search millions of evidence-based medical sources directly within your workflow. • Diagnostics AI - Access AI-powered clinical tools designed to support patient care. • One Connected Workflow Move seamlessly between documentation, research, and clinical insights without interrupting your consult. Designed For • Physicians • Nurse Practitioners • Physician Assistants • Residents • Medical Students • Specialists • Primary Care Why Keikku Modern healthcare requires more than a single AI tool. Keikku combines documentation, clinical reference, and intelligent clinical workflows into one AI Clinical Platform built for everyday practice. Download Keikku and explore the platform for free. Disclaimer: The Keikku device is not a substitute for professional medical advice, diagnosis, or treatment. Please consult a doctor before making any medical decisions based on the information provided by this app. Regulatory Information: The Keikku Electronic Stethoscope is an FDA-cleared Class II medical device (510(k) K233313) authorized for marketing in the United States. It is intended for use on pediatric and adult patients by professional users in a clinical environment or by lay users in a nonclinical environment. The device is not intended for self-diagnosis. Outside the United States, the Keikku device is for investigational use only. A clinical trial is currently registered and active in Peru (ClinicalTrials.gov ID: NCT07044128). CE marking under the EU Medical Device Regulation (MDR 2017/745) is in progress. Users outside the United States will see an investigational use disclaimer within the app. Always consult a qualified healthcare professional before making any medical decisions.