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American Medical Solutions LLC

US

Last updated May 31, 2026

What American Medical Solutions LLC makes

American Medical Solutions LLC manufactures portable electronic sphygmomanometers designed for automatic inflation, intended for use on the arm or wrist. These devices are primarily used to measure blood pressure in clinical and home settings, providing digital readings for monitoring cardiovascular health.

The company’s products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within the United States, adhering to applicable medical device compliance standards for blood pressure measurement devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does American Medical Solutions LLC manufacture?

American Medical Solutions LLC specializes in portable electronic sphygmomanometers that automatically inflate. These devices are designed for use on either the arm or wrist and are primarily intended for measuring blood pressure in both clinical and home settings. Their focus is on digital blood pressure monitoring to support cardiovascular health assessment.

Where is American Medical Solutions LLC based?

American Medical Solutions LLC is based in the United States. The company operates within the country’s regulatory framework, ensuring compliance with applicable standards for medical devices, particularly those related to blood pressure measurement.

Which regulatory registries or databases list American Medical Solutions LLC’s devices?

American Medical Solutions LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are American Medical Solutions LLC’s devices classified by regulatory authorities?

American Medical Solutions LLC’s devices fall under FDA Class II classification. This classification is assigned based on the risk level of the device—Class II devices generally pose moderate risks and require special controls in addition to general controls to ensure safety and effectiveness, such as automatic-inflation sphygmomanometers.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Email
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
118331001

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Ams Proof JPD-HA101
FDA UDI
Class IIActive

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