Not currently registered with FDA under this name

Msi France

Paris, France. Named as applicant on 1 dental 510(k) clearance between 2018 and 2018. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 12018–2018
Markets registered in: 21 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Msi France as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: FranceOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Msi France	1 clearances	2018–2018	Below
Hong Kong	MDD	Manufacturer	MSI France sas	1	2021–2021	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Msi France as the applicant.

Decided	510(k)	Device	Device type
31 Jan 2018	K172240	SPI Dental Implant System	DZE Root-Form Endosseous Implant

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.