Manufacturer registered with FDA

Safari Dental, Inc.

BOISBRIAND, QUEBEC, Canada. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator9027483Manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
12010–2010
Markets registered in
23 registrations outside the US
Establishments
1Canada
2010: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Safari Dental, Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedCanada: 3 registrations
RegisteredHome: CanadaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSafari Dental, Inc.1 clearances2010–2010Below
CanadaHealth CanadaRegistration holderSAFARI DENTAL INC.32007–2014Pure 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 Safari Dental, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Operating LightEAZ · Class 1Dental operating lightsMaker
REFLECTED LIGHT
2006
Operative Dental UnitEIA · Class 1Dental chairs & operative unitsMaker
Operative Dental Unit
2011

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

510(k) clearances

Clearances on which FDA names Safari Dental, Inc. as the applicant.

Decided510(k)DeviceDevice type
22 Oct 2010K100212DENTACENTER/EXPEDITION, MODEL SAF-430EIA Operative Dental Unit

Registered establishments

EstablishmentLocationWhat it does
SAFARI DENTAL, INC.FDA reg. 9681829BOISBRIAND Quebec, CanadaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9027483). 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.