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Advantage Medical Systems, Inc.

United StatesFDA applicant, unverified

Devices
17

What Advantage Medical Systems, Inc. makes

Advantage Medical Systems, Inc. manufactures medical monitoring devices, including fetal and neonatal physiological monitors, telemetry systems for remote data transmission, and electrographic monitoring equipment. Their product line also covers non-coring Huber-type needles and laser positioning devices for surgical applications. Additional offerings include tocometry data transmitters and Holter screening monitors for continuous cardiac rhythm assessment.

The company’s devices are regulated under FDA’s 510(k) pathway, with products classified as Class I and Class II. Their equipment is listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Advantage Medical Systems, Inc. have in the registry?

The registry currently lists 17 devices for Advantage Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Advantage Medical Systems, Inc.'s devices?

Among its 17 most recently registered devices, Advantage Medical Systems, Inc. has devices listed in FDA 510(k) (17 devices).

What risk classes do Advantage Medical Systems, Inc.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Advantage Medical Systems, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Advantage Medical Systems, Inc. in the registry?

The most recently registered devices listed for Advantage Medical Systems, Inc. include FETAL MONITOR MODEL FHM-1, NON-CORING HUBER TYPE NEEDLES, CENTRAL DISPLAY SYSTEM #CS400 and WALL MOUNTED LASER POSITIONING DEVICE.

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