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Devon Industries, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
47

What Devon Industries, Inc. makes

Devon Industries, Inc. manufactures reusable and disposable surgical accessories, including magnetic instrument holders for drapes, sponge counters for inventory tracking, and electrosurgical tip cleaners and holders. Their portfolio also covers sharps management solutions like the Sharps Collection and Disposal System and needle protection devices, such as the Point Lok Needle Protection Device. Additional products include adhesive traction tape, phlebotomy unit sharps containment, surgical rulers with pens, and reusable instrument protectors like the Hibernation Kit and DEVO’N Loops.

The company’s devices are regulated under FDA Class I and Class II classifications, with most products requiring 510(k) clearance. These items are listed in the FDA’s 510(k) registry, and the manufacturer operates from 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 Devon Industries, Inc. have in the registry?

The registry currently lists 47 devices for Devon Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Devon Industries, Inc.'s devices?

Among its 47 most recently registered devices, Devon Industries, Inc. has devices listed in FDA 510(k) (47 devices).

What risk classes do Devon Industries, Inc.'s devices fall under?

Among its 47 most recently registered devices, the classes recorded for Devon Industries, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Devon Industries, Inc. in the registry?

The most recently registered devices listed for Devon Industries, Inc. include MAGNETIC DRAPE - INSTRUMENT HOLDER, SPONGE COUNTER, ELECTROSURGICAL TIP CLEANER & HOLDER and SURGICAL INSTRUMENT PROTECTOR.

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