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Moving Islands Transit Inc

US

Last updated May 31, 2026

What Moving Islands Transit Inc makes

Moving Islands Transit Inc manufactures reusable dental impression material kits designed for crown and bridge procedures. Their portfolio includes specialized systems for anterior, posterior, and introductory crown and bridge applications, providing clinicians with tools for capturing precise dental impressions.

The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Moving Islands Transit Inc manufacture?

Moving Islands Transit Inc specializes in reusable dental impression material kits. These kits are specifically designed for crown and bridge procedures, including systems tailored for anterior (front teeth), posterior (back teeth), and introductory crown and bridge applications. The focus is on providing precise dental impression solutions for clinicians.

Where is Moving Islands Transit Inc based?

Moving Islands Transit Inc is headquartered in the United States. The company’s location is relevant for understanding its regulatory context, as it operates under U.S. medical device regulations.

Which regulatory registries list the devices manufactured by Moving Islands Transit Inc?

The devices produced by Moving Islands Transit Inc are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify Class II devices, ensuring transparency and traceability in the medical device supply chain.

How are the devices from Moving Islands Transit Inc classified under U.S. regulations?

The dental impression material kits from Moving Islands Transit Inc fall under Class II classification according to FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as validation of manufacturing processes and performance testing.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
miticbs.com
LinkedIn
—
Facebook
—
Phone
1-855-900-6484
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
202781316

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Anterior Crown and Bridge Impression System Kit 627843379584
FDA UDI
Class IIActive
Posterior Crown and Bridge Impression System Kit 627843379591
FDA UDI
Class IIActive
Introduction Crown and Bridge Impression System Kit 627843379621
FDA UDI
Class IIActive

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