Manufacturer registered with FDA
Veden Dental Labs Inc
Zhuhai, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 440 registrations outside the US
- Establishments
- 1China
Registered in 4 markets
Where regulators' registries name Veden Dental Labs Inc 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 | Veden Dental Labs Inc | 1 device types | — | Below |
| United Kingdom | MHRA | Manufacturer | Veden Dental Labs Inc. | 26 | — | Pure Global AI |
| Canada | Health Canada | Registration holder | VEDEN DENTAL LABS, INC. | 10 | 2014–2019 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | VEDEN DENTAL LABS INCVeden Dental Labs Inc. | 4 | 2009–2025 | 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 Veden Dental Labs Inc currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Orthodontic Screw Expansion RetainerDYJ · Class 1 | Retainers, expanders & headgear | Maker | NTl Splint,Essix Retainer; Bleaching Tray; Night Guard; Sports Guard; Study Model; TPA retainer; Begg Retainer;Palatel Expander; Quad HelixSpring Hawley; Spring Appliance; Hawley Retainer; Space Maintainer; Nannce Appliance; Lingual Retainer; Thumb Crib; | 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 |
|---|---|---|
| VEDEN DENTAL LABS INCFDA reg. 3007603956 | Zhuhai Guangdong, China | Contract manufacturer, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10030301). 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.