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Hoffrel Instruments, Inc.

United StatesFDA applicant, unverified

Devices
12

What Hoffrel Instruments, Inc. makes

Hoffrel Instruments, Inc. manufactures ultrasonic diagnostic systems and associated transducers, including mechanical sector scanning drives and Doppler-equipped ultrasonoscopes. Their portfolio includes standalone diagnostic systems like the Vascular Profile System and Ultrasonic Diagnostic System, as well as specialized transducers (e.g., models 420, 421, 450–454) designed for compatibility with external imaging platforms. Additional components like motor drives for mechanical scanning are also part of their offerings.

The company’s devices fall under Class II regulatory classification in the US, with most products authorised via 510(k) clearance through the FDA. Their portfolio is listed in the FDA 510(k) registry, reflecting compliance with US medical device regulations. The manufacturer operates from the United States.

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

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Frequently asked questions

How many devices does Hoffrel Instruments, Inc. have in the registry?

The registry currently lists 12 devices for Hoffrel Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hoffrel Instruments, Inc.'s devices?

Among its 12 most recently registered devices, Hoffrel Instruments, Inc. has devices listed in FDA 510(k) (12 devices).

What risk classes do Hoffrel Instruments, Inc.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Hoffrel Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hoffrel Instruments, Inc. in the registry?

The most recently registered devices listed for Hoffrel Instruments, Inc. include MODEL VPS VASCULAR PROFILE SYSTEM, ULTRASONIC DIAGNOSTIC SYSTEM, MOD. 202, TRANSDUCERS MODELS 421, 419 AND 420 FOR IREX SYSTEM and MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417.

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