Manufacturer registered with FDA
Seplou (Zhuhai) Co.,ltd.
Zhuhai, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 67 registrations outside the US
- Establishments
- 1China
Registered in 6 markets
Where regulators' registries name Seplou (Zhuhai) 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 | Seplou (Zhuhai) Co.,ltd. | 1 device types | — | Below |
| Brazil | ANVISA | Manufacturer | SEPLOU (ZHUHAI)CO., LTD | 2 | 2026–2026 | Pure Global AI |
| South Korea | MFDS | Manufacturer | SEPLOU (ZHUHAI) CO., LTDSEPLOU (ZHUHAI) CO., LTD. | 2 | 2025–2026 | Pure Global AI |
| Hong Kong | MDD | Manufacturer | SEPLOU (ZHUHAI) CO., LTD. | 1 | 2026–2026 | Pure Global AI |
| Peru | DIGEMID | Manufacturer | SEPLOU (ZHUHAI) CO., LTD. | 1 | 2026–2026 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | SEPLOU (ZHUHAI) CO., LTD. | 1 | 2026–2026 | 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 Seplou (Zhuhai) 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 | — | 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 |
|---|---|---|
| SEPLOU (ZHUHAI) CO.,LTD.FDA reg. 3035480112 | Zhuhai Guangdong, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10092239). 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.