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Hommed, LLC

United StatesFDA applicant, unverified

Devices
8

What Hommed, LLC makes

Hommed, LLC manufactures patient monitoring systems, including standalone units like the Hommed Sentry IIIB-F and Hommed Observer (Model I), as well as central station solutions such as the Central Station (Version 3.3H) for aggregating and managing patient data. Options include add-ons like card readers for the Sentry III series, designed for real-time vital sign tracking in clinical settings.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States, adhering to U.S. medical device compliance standards.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Hommed, LLC have in the registry?

The registry currently lists 8 devices for Hommed, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hommed, LLC's devices?

Among its 8 most recently registered devices, Hommed, LLC has devices listed in FDA 510(k) (8 devices).

What risk classes do Hommed, LLC's devices fall under?

Among its 8 most recently registered devices, the classes recorded for Hommed, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hommed, LLC in the registry?

The most recently registered devices listed for Hommed, LLC include HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS, CENTRAL STATION, VERSION 3.3H, HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM and HOMMED OBSERVER, MODEL I.

Generated automatically from registry data and not verified by a human reviewer.