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E M F

US

Last updated May 25, 2026

What E M F makes

E M F manufactures dental mirrors, specifically reusable ones, with products such as RIOFOTO. These dental mirrors are used for examining the mouth and teeth. The company's product portfolio consists of this type of dental device.

The company's devices are classified as Class I and are listed in the FDA UDI registry. E M F is based in the US. The devices are subject to regulatory oversight in the country where they are marketed.

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

Frequently asked questions

What does E M F make?

E M F manufactures reusable dental mirrors, with products such as RIOFOTO, which are used for examining the mouth and teeth during dental procedures.

Where is E M F based?

E M F is based in the United States, as indicated by the country field in the device data.

Which regulatory registry lists E M F's devices?

E M F's devices are listed in the FDA UDI registry, which is the Unique Device Identification system maintained by the U.S. Food and Drug Administration.

How are E M F's devices classified?

E M F's devices are classified as Class I, which indicates they are subject to general controls and represent the lowest risk category under FDA device classification.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
002234375

Catalogue (12)

DeviceModel / ReferenceRegistriesClassStatus
Riofoto 2A
FDA UDI
Class IActive
Riofoto 4A
FDA UDI
Class IActive
Riofoto 2C
FDA UDI
Class IActive
Riofoto 1A
FDA UDI
Class IActive
Riofoto 1B
FDA UDI
Class IActive
Riofoto 2B
FDA UDI
Class IActive
Riofoto 4C
FDA UDI
Class IActive
Riofoto 3BC
FDA UDI
Class IActive
Riofoto 3A
FDA UDI
Class IActive
Riofoto 1C
FDA UDI
Class IActive
Riofoto 3C
FDA UDI
Class IActive
Riofoto 3B
FDA UDI
Class IActive

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