AI devices with FDA product code MWI — Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Product code MWI (“Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)” in openFDA) covers 5 devices on the FDA AI-enabled list, from 4 companies. Most are reviewed by the Cardiovascular panel (5). The most recent decision was Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care Portal on June 6, 2025.
5AI devices
4Companies
2018First decision
2025-06-06Latest decision
Trend: devices per year
2018201920202025
Top companies
All 5 devices, newest first
- Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care PortalEmpatica S.R.L. · Cardiovascular
- Eko Analysis SoftwareEko Devices Inc · Cardiovascular
- PeraMobile and PeraWatchPeraHealth, Inc. · Cardiovascular
- PeraServer and PeraTrendPeraHealth, Inc. · Cardiovascular
- WAVE Clinical PlatformExcel Medical Electronics, LLC · Cardiovascular