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Amico Diagnostic Incorporated

Country not established FDA

Devices
260
Registrations
FDA
FDA recalls
0

Catalogue260

Newest first, page 6 of 6

Showing 251-260 of 260

Company details

DUNS number
203163290
Phone
1-877-264-2697

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Amico Diagnostic Incorporated Richmond Hill Ontario · CA FEI 3009685433

What Amico Diagnostic Incorporated makes

Amico Diagnostic Incorporated manufactures manual and electronic blood pressure measurement devices, including aneroid sphygmomanometers, reusable blood pressure cuffs, and manual cuff inflators. Their portfolio also includes direct ophthalmoscopes for eye examinations and patient thermometers, such as intermittent electronic and infrared (ear) models. Some products are designed for clinical use, such as wall-mounted stations and rollstands for blood pressure monitoring, while others are standalone components like cuffs and cuff inflators.

The company’s devices are regulated under the US Food and Drug Administration (FDA) as Class I and Class II medical devices, with some authorised through the 510(k) premarket notification process and others listed under the Unique Device Identifier (UDI) system. These products are intended for use in clinical, home, and professional settings, adhering to FDA compliance requirements for their respective classifications.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.