Not currently registered with FDA under this name

Ilerimplant S.L

Lleida, Spain. Named as applicant on 1 dental 510(k) clearance between 2017 and 2017. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12017–2017
Markets registered in
225 registrations outside the US
Establishments
0—
2017: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Ilerimplant S.L as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesCosta Rica: 25 registrations
RegisteredHome: SpainOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantIlerimplant S.L1 clearances2017–2017Below
Costa RicaMinisterio de SaludManufacturerIlerimplant S.L25—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 Ilerimplant S.L as the applicant.

Decided510(k)DeviceDevice type
19 Jan 2017K161593GMI Frontier Dental Implant SystemDZE Root-Form Endosseous Implant

Some of these clearances are listed with FDA today by another company: GMI Dental Implantology, S.L. (1).

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.