Manufacturer registered with FDA
Nanning VV Dental Co., Ltd.
Nanning, China. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 12017–2017
- Markets registered in
- 310 registrations outside the US
- Establishments
- 1China
510(k) clearances per year, 2007–2026
Registered in 3 markets
Where regulators' registries name Nanning VV Dental Co., 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 | Nanning VV Dental Co., Ltd. | 1 clearances | 2017–2017 | Below |
| Brazil | ANVISA | Manufacturer | NANNING VV DENTAL CO. LTD.NANNING V V DENTAL CO., LTD | 7 | 2017–2026 | Pure Global AI |
| South Korea | MFDS | Manufacturer | NANNING VV DENTAL Co., Ltd.NANNING V V DENTAL CO.,LTD. | 3 | 2014–2018 | 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 Nanning VV Dental Co., 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 |
|---|---|---|---|---|
| Ultrasonic ScalerELC · Class 2 | Ultrasonic scalers | Maker | Scaler,ultrasonic E2,P2,SK-E1,SK-D1Scaler,ultrasonic VET-1,VET-W3,VET-W3-LED,VET-6,WET-6-LED,VET-W7,WET-W7-LED,VST-1,VST-W3,VST-6,VST-W7 | 2018 |
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 |
|---|---|---|
| NANNING VV DENTAL CO., LTD.FDA reg. 3014315145 | Nanning Guangxi, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10056843). 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.