Manufacturer registered with FDA
Meta Biomed Vina One member Limited Liability Company
Can Giuoc District, Vietnam. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 23 registrations outside the US
- Establishments
- 1Vietnam
Registered in 2 markets
Where regulators' registries name Meta Biomed Vina One member Limited Liability Company 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 | Meta Biomed Vina One member Limited Liability Company | 2 device types | — | Below |
| Taiwan | TFDA | Manufacturer | META BIOMED VINA ONE MEMBER LIMITED LIABILITY COMPANYMeta Biomed Vina One Member Limited Liability Company | 3 | 2020–2021 | 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 Meta Biomed Vina One member Limited Liability Company currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Gutta-PerchaEKM · Class 1 | Root canal filling materials | Maker | GUTTA-PERCHA | 2017 |
| Endodontic Paper PointEKN · Class 1 | Root canal filling materials | Maker | Endodontic Point Paper | 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 |
|---|---|---|
| META BIOMED VINA ONE MEMBER LIMITED LIABILITY COMPANYFDA reg. 3014159752 | Can Giuoc Commune Tay Ninh, Vietnam | Contract manufacturer, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10056383). 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.