Manufacturer registered with FDA

Incisive Technologies Pty Ltd

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

FDA owner/operator10091851Manufacturer1 clearance in five years
Device types listed
1
Brands and models
1
510(k) clearances
12023–2023
Markets registered in
21 registrations outside the US
Establishments
1Australia
2023: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Incisive Technologies Pty Ltd as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedAustralia: 1 registrations
RegisteredHome: AustraliaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerIncisive Technologies Pty Ltd1 clearances2023–2023Below
AustraliaTGAManufacturerIncisive Technologies Pty Ltd12024–2024Pure 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 Incisive Technologies Pty Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Caries Detection DeviceLFC · Class 2Caries detection devicesMaker
BlueCheck
2024

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 Incisive Technologies Pty Ltd as the applicant.

Decided510(k)DeviceDevice type
16 May 2023K222560BlueCheck™ Caries Detection & MonitoringLFC Caries Detection Device

Registered establishments

EstablishmentLocationWhat it does
Incisive Technologies Pty LtdFDA reg. 3033588343Ferntree Gully Victoria, AustraliaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10091851). 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.