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Emoled, Srl

ItalyFDA 510(k) applicant, unverified FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Emoled, Srl makes

Emoled, Srl manufactures the EmoLED device, a Class II medical product.

The EmoLED is listed in the FDA 510(k) registry, and the company is based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • EmoLED (v. 2-USA) Ref K240132

    Class II
    Active 510(k) 510(k) II

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Emoled SRL Sesto Fiorentino Firenze · IT FEI 3025861981

Frequently asked questions

How many devices does Emoled, Srl have in the registry?

The registry currently lists 1 device for Emoled, Srl. Devices recorded under merged duplicate company entries are counted once.

Which registries list Emoled, Srl's devices?

Among its 1 most recently registered device, Emoled, Srl has devices listed in FDA 510(k) (1 device).

What risk classes do Emoled, Srl's devices fall under?

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

What are the newest devices from Emoled, Srl in the registry?

The most recently registered devices listed for Emoled, Srl include EmoLED (v. 2-USA).

Which FDA establishments are linked to Emoled, Srl?

1 FDA establishment is linked to Emoled, Srl in the registry; they are listed on the company page.

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