AI devices with FDA product code DQD — Stethoscope, Electronic
Product code DQD (“Stethoscope, Electronic” in openFDA) covers 14 devices on the FDA AI-enabled list, from 13 companies. Most are reviewed by the Cardiovascular panel (14). The most recent decision was Tyto Stethoscope (G3) on March 12, 2026.
14AI devices
12Companies
2012First decision
2026-03-12Latest decision
Trend: devices per year
201220132016201920202022202320252026
Top companies
All 14 devices, newest first
- Tyto Stethoscope (G3)Tyto Care , Ltd. · Cardiovascular
- Kneevoice Cartilage Evaluation System (750-3600-001)Kneevoice, Inc. · Cardiovascular
- eMurmur Heart AICsd Labs · Cardiovascular
- Stethophone ProSparrow Acoustics, Inc. · Cardiovascular
- Eko Foundation Analysis Software with Transformers (EFAST)Eko Health, Inc. · Cardiovascular
- AusculThing ACCAusculThing Oy · Cardiovascular
- Eko Murmur Analysis Software (EMAS)Eko Devices, Inc. · Cardiovascular
- eMurmur Heart AICSD Labs GmbH · Cardiovascular
- Stethee Pro 1, Stethee Pro Software SystemM3DICINE Pty Ltd. · Cardiovascular
- eMurmur IDCSD Labs GmbH · Cardiovascular
- Tyto StethoscopeTyto Care Ltd. · Cardiovascular
- Steth IOSTRATOSCIENTIFIC, INC. · Cardiovascular
- SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATIONDIACOUSTIC MEDICAL DEVICES (PTY) LTD. · Cardiovascular
- SENSICARDIACDIACOUSTIC MEDICAL (PTY) · Cardiovascular