Manufacturer registered with FDA
Ningbo Seago Electric Co.,Ltd
Ningbo, China. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 348 registrations outside the US
- Establishments
- 1China
Registered in 3 markets
Where regulators' registries name Ningbo Seago Electric 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 | Ningbo Seago Electric Co.,Ltd | 4 device types | — | Below |
| Canada | Health Canada | Registration holder | NINGBO SEAGO ELECTRIC CO., LTD. | 43 | 2009–2026 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | NINGBO SEAGO ELECTRIC CO., LTD. | 5 | — | 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 Ningbo Seago Electric 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 |
|---|---|---|---|---|
| Oral Irrigation UnitEFS · Class 1 | Oral irrigators | Maker | — | 2019 |
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | — | 2009 |
| Powered ToothbrushJEQ · Class 1 | Toothbrushes | Maker | — | 2009 |
| Sterile Ultraviolet Sanitation/Sterilization (for Toothbrushes) UnitMCF · Class 1 | — | Maker | — | 2009 |
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 |
|---|---|---|
| NINGBO SEAGO ELECTRIC CO.,LTDFDA reg. 3006115534 | Ningbo Zhejiang, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10028829). 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.