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Sillard Products, Inc.

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Devices
1

What Sillard Products, Inc. makes

Sillard Products, Inc. manufactures ceramic-based metal alloy devices designed for medical applications, including orthopedic and dental implants.

These products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Ceral-Base Metal Alloy Ref K813243

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Sillard Products, Inc. have in the registry?

The registry currently lists 1 device for Sillard Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sillard Products, Inc.'s devices?

Among its 1 most recently registered device, Sillard Products, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Sillard Products, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Sillard Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sillard Products, Inc. in the registry?

The most recently registered devices listed for Sillard Products, Inc. include CERAL-BASE METAL ALLOY.

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