Skip to content

Morningstar Dental Co.

Country not established

Devices
1

What Morningstar Dental Co. makes

Morningstar Dental Co. manufactures PlasticEph, a dental device designed for temporary or permanent restorative applications in dentistry, likely including crowns, bridges, or inlays made from plastic-based materials.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The device is listed in the FDA’s 510(k) database. The manufacturer 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

  • Plasticeph Ref K810538

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

Frequently asked questions

How many devices does Morningstar Dental Co. have in the registry?

The registry currently lists 1 device for Morningstar Dental Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Morningstar Dental Co.'s devices?

Among its 1 most recently registered device, Morningstar Dental Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Morningstar Dental Co.'s devices fall under?

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

What are the newest devices from Morningstar Dental Co. in the registry?

The most recently registered devices listed for Morningstar Dental Co. include PLASTICEPH.

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