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Internet of Medical Things (IoMT): Connected Health Devices

Connected medical devices, wearables and health data systems — with the standards, cloud platforms, security tools and regulators that shape them.

80 topics•8 categories•Updated October 2026

What Is the IoMT?

6 entries

The Internet of Medical Things (IoMT) is the connected network of medical devices, wearables, sensors and software that collect, send and analyse health data. Examples include continuous glucose monitors, connected infusion pumps, patient monitors, cardiac patches and imaging systems that feed electronic health records and cloud analytics. It supports remote patient monitoring and faster clinical decisions, but it also adds risks: device security, data privacy, interoperability and regulatory compliance.

Connected Devices & Wearables

16 entries

Makers of monitors, patches, sensors and imaging systems.

Interoperability & Data Standards

15 entries

How device and health data are exchanged and coded.

Cloud & Health Data Platforms

6 entries

Managed services for storing and analysing health data.

Medical Device Security

11 entries

Protecting connected devices and patient data.

Regulation & Policy

11 entries

Rules for devices and health data.

News & Trade Publications

5 entries

Stay current.

Related Pages

10 entries

Neighbouring pages on this site.

Frequently Asked Questions

What is the Internet of Medical Things (IoMT)?

The IoMT is the network of connected medical devices, wearables, sensors and software that collect, transmit and analyse health data, supporting remote monitoring, clinical decisions and connected care.

Which standards matter for IoMT?

HL7 FHIR is the main API standard for health data, DICOM covers medical imaging, IEEE 11073 and Bluetooth profiles cover personal health devices, and SNOMED CT and LOINC provide clinical codes.

What are the main security and privacy concerns?

Connected devices can have unpatched software, weak authentication and long lifetimes, and they carry sensitive patient data. Regulators such as the FDA and rules such as HIPAA and the EU MDR set expectations for device security and data protection.

Which regulations apply?

It depends on where a device is sold and used: the FDA and HIPAA in the United States, the EU MDR and data protection law in Europe, and CDSCO and ABDM in India. Confirm requirements with the regulator or counsel.

How current is this page?

Links were checked in October 2026. Regulatory pages, product claims and company ownership change often; this page is an information directory, not medical, legal or compliance advice, so confirm requirements with the regulator or vendor. Sites that block automated checks (including the FDA) are kept and may need a manual click.