Manufacturer registered with FDA
LargeV Instrument Corp., Ltd.
Beijing, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 69 registrations outside the US
- Establishments
- 1China
Registered in 6 markets
Where regulators' registries name LargeV Instrument Corp., Ltd. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | LargeV Instrument Corp., Ltd. | 1 device types | — | Below |
| European Union | EUDAMED | Manufacturer | LargeV Instrument Corp., Ltd. | 4 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | LargeV Instrument Corp. Ltd. | 2 | 2016–2019 | Pure Global AI |
| Australia | TGA | Manufacturer | LargeV Instrument Corp Ltd | 1 | 2021–2021 | Pure Global AI |
| Costa Rica | Ministerio de Salud | Manufacturer | LargeV Instrument Corp. Ltd. | 1 | — | Pure Global AI |
| Peru | DIGEMID | Manufacturer | LARGEV INSTRUMENT CORP. LTD. | 1 | 2022–2022 | 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 LargeV Instrument Corp., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Computer Assisted Design and Manufacturing (Cad/Cam) of Dental Restorations Optical Impression SystemNOF · Class 2 | Intraoral scanners | Maker | Intraoral Scanner, FusionScanner SU, FusionScanner SU Lab, FusionScanner SU Pro | 2025 |
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
| Establishment | Location | What it does |
|---|---|---|
| LARGEV INSTRUMENT CORP., LTD.FDA reg. 3038590535 | Beijing, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10094464). 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.