Registered with FDA

Process For Prf Sarl

Nice, France. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10045262Private-label distributor
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
410 registrations outside the US
Establishments
1France

Registered in 4 markets

Where regulators' registries name Process For Prf Sarl as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedTaiwan: 6 registrationsBrazil: 3 registrationsCosta Rica: 1 registrations
RegisteredHome: FranceOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAListerProcess For Prf Sarl2 device types—Below
TaiwanTFDAManufacturerPROCESS FOR PRF S.A.R.L62015–2021Pure Global AI
BrazilANVISAManufacturerPROCESS FOR PRF32019–2019Pure Global AI
Costa RicaMinisterio de SaludManufacturerPROCESS FOR PRF1—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 Process For Prf Sarl currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Surgical Tissue ScissorsEGN · Class 1Dental hand instrumentsLister
A-PRF Scissors
2015
Dental Surgical ElevatorEMJ · Class 1Dental hand instrumentsLister
Soft Tissue Brush
2018

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
PROCESS FOR PRF SARLFDA reg. 3007006186Nice Alpes-Maritimes, FrancePrivate-label distributor

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10045262). 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.