Manufacturer registered with FDA
Ming Fai Enterprise (Cambodia) Co.,LTD
Samraong Tong, Cambodia. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 32 registrations outside the US
- Establishments
- 1Cambodia
Registered in 3 markets
Where regulators' registries name Ming Fai Enterprise (Cambodia) 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 | Ming Fai Enterprise (Cambodia) Co.,LTD | 3 device types | — | Below |
| South Korea | MFDS | Manufacturer | MING FAI ENTERPRISE (CAMBODIA) CO., LTD. | 1 | 2014–2014 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | Ming Fai Enterprise (Cambodia) Co., Ltd. | 1 | 2025–2025 | 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 Ming Fai Enterprise (Cambodia) 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 |
|---|---|---|---|---|
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | — | 2019 |
| Dental FlossJES · Class 1 | Floss & interdental cleaners | Maker | — | 2024 |
| Dental Hygiene KitNXZ · Class 1 | — | Maker | — | 2019 |
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 |
|---|---|---|
| MING FAI ENTERPRISE (CAMBODIA) CO.,LTDFDA reg. 3015531959 | Samraong Tong District Kampong Speu, Cambodia | Contract manufacturer, Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10060734). 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.