Eufoton S.R.L.
ItalyFDA 510(k) applicant, unverified FDA FEI 3005403788
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Eufoton S.R.L. makes
Eufoton S.R.L. manufactures laser devices, including the LASEMAR series, which comprises models such as the 800, 1000, and 1500. These devices are medical in nature, indicating their intended use in healthcare settings. The company's products are specifically categorized as laser devices.
The portfolio of Eufoton S.R.L. is regulated under Class II devices and is listed in the FDA 510(k) registry. The company is based in the US. Its devices are subject to the regulatory oversight of the FDA, ensuring compliance with relevant medical device standards.
Catalogue
Lasemar 800, 1000, 1500 Ref K092860
510(k) 510(k)
Company details
- FDA FEI number
- 3005403788
- Address
- via Flavia 23/1, Trieste
Frequently asked questions
How many devices does Eufoton S.R.L. have in the registry?
The registry currently lists 1 device for Eufoton S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eufoton S.R.L.'s devices?
Among its 1 most recently registered device, Eufoton S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Eufoton S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eufoton S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eufoton S.R.L. in the registry?
The most recently registered devices listed for Eufoton S.R.L. include LASEMAR 800, 1000, 1500.