Manufacturer registered with FDA

ClearMoves Aligners

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

FDA owner/operator10091513Manufacturer1 clearance in five years
Device types listed
1
Brands and models
1
510(k) clearances
12024–2024
Markets registered in
35 registrations outside the US
Establishments
1Pakistan
2024: 120102020

510(k) clearances per year, 2007–2026

Registered in 3 markets

Where regulators' registries name ClearMoves Aligners as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedUnited Kingdom: 4 registrationsAustralia: 1 registrations
RegisteredHome: PakistanOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerClearMoves Aligners1 clearances2024–2024Below
United KingdomMHRAManufacturerCLEAR MOVES ALIGNERS LTDClear Moves Aligners4—Pure Global AI
AustraliaTGAManufacturerClear Moves Aligners Pty LtdClearmoves Aligners12023–2023Pure 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 ClearMoves Aligners currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Sequential AlignerNXC · Class 2Clear alignersMaker
Clear Moves Aligner
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 ClearMoves Aligners as the applicant.

Decided510(k)DeviceDevice type
1 Aug 2024K241137Clear Moves AlignerNXC Sequential Aligner

Registered establishments

EstablishmentLocationWhat it does
CLEARMOVES ALIGNERSFDA reg. 3033508190Lahore Punjab, PakistanManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10091513). 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.