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Mon-A-Therm, Inc.

United StatesFDA applicant, unverified

Devices
17

What Mon-A-Therm, Inc. makes

Mon-A-Therm, Inc. manufactures temperature monitoring devices, including disposable and reusable sensors for skin, modified airways, Foley catheters, esophageal stethoscopes, tympanic/rectal/esophageal sites, and anesthesia breathing circuits. The portfolio also includes temperature trend indicators, subcutaneous sensors, and adapter systems for integrating temperature measurement into existing medical equipment.

These devices are classified under FDA’s Class I and Class II regulations, with most requiring 510(k) clearance. The company’s products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Mon-A-Therm, Inc. have in the registry?

The registry currently lists 17 devices for Mon-A-Therm, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mon-A-Therm, Inc.'s devices?

Among its 17 most recently registered devices, Mon-A-Therm, Inc. has devices listed in FDA 510(k) (17 devices).

What risk classes do Mon-A-Therm, Inc.'s devices fall under?

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

What are the newest devices from Mon-A-Therm, Inc. in the registry?

The most recently registered devices listed for Mon-A-Therm, Inc. include MON-A-THERM'S SKIN TEMPERATURE SENSOR, MODIFIED AIRWAY TEMPERATURE SENSOR, MODIFIED FOLEY CATHETER/TEMPERATURE SENSOR and MODIFIED ESOPHAGEAL STETHOSCOPE/TEMPERATURE SENSOR.

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