Manufacturer registered with FDA

Navigate Surgical Technologies Inc.

Vancouver, Canada. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10084472Manufacturer1 clearance in five years
Device types listed
1
Brands and models
1
510(k) clearances
12022–2022
Markets registered in
225 registrations outside the US
Establishments
1Canada
2022: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Navigate Surgical Technologies Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedCanada: 25 registrations
RegisteredHome: CanadaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerNavigate Surgical Technologies Inc.1 clearances2022–2022Below
CanadaHealth CanadaRegistration holderNAVIGATE SURGICAL TECHNOLOGIES, INC.252015–2019Pure 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 Navigate Surgical Technologies Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Stereotaxic InstrumentPLV · Class 2—Maker
INLIANT® Surgical Navigation System
2022

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 Navigate Surgical Technologies Inc. as the applicant.

Decided510(k)DeviceDevice type
22 Feb 2022K213392INLIANT Surgical Navigation SystemPLV Dental Stereotaxic Instrument

Registered establishments

EstablishmentLocationWhat it does
NAVIGATE SURGICAL TECHNOLOGIES INC.FDA reg. 3021736516Vancouver British Columbia, CanadaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10084472). 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.