Manufacturer registered with FDA

MG Developpement

mauguio, France. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10025161Foreign exporterManufacturer
Device types listed
1
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
423 registrations outside the US
Establishments
1France

Registered in 4 markets

Where regulators' registries name MG Developpement as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedAustralia: 10 registrationsUnited Kingdom: 10 registrationsEuropean Union: 3 registrations
RegisteredHome: FranceOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerMG Developpement1 device types—Below
AustraliaTGAManufacturerMG Developpement102019–2019Pure Global AI
United KingdomMHRAManufacturerMG Developpement10—Pure Global AI
European UnionEUDAMEDManufacturerMG DEVELOPPEMENT3—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

Devices listed with FDA

What MG Developpement currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Silicate ProtectorEFX · Class 1—Maker—2008

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
MG DEVELOPPEMENTFDA reg. 3006979687mauguio Herault, FranceForeign exporter, Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10025161). 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.