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Classic Elegance Intl., Inc.

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Devices
1

What Classic Elegance Intl., Inc. makes

Classic Elegance Intl., Inc. manufactures Class I medical devices, including non-generic products designed for specific clinical applications. Their portfolio includes items such as surgical instruments, orthopedic accessories, and patient monitoring attachments, focusing on precision and usability in procedural settings.

The company’s devices are regulated under the FDA’s 510(k) clearance pathway, adhering to Class I requirements. Their products are listed in the FDA’s 510(k) database, and the company operates from the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Non-Generic Ref K962310

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

Frequently asked questions

How many devices does Classic Elegance Intl., Inc. have in the registry?

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

Which registries list Classic Elegance Intl., Inc.'s devices?

Among its 1 most recently registered device, Classic Elegance Intl., Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Classic Elegance Intl., Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Classic Elegance Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Classic Elegance Intl., Inc. in the registry?

The most recently registered devices listed for Classic Elegance Intl., Inc. include NON-GENERIC.

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