Manufacturer registered with FDA
Shenzhen Baofengtong Electrical Appliances Manufacturing Co.
Shenzhen, China. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 38
- 510(k) clearances
- 0as applicant
- Markets registered in
- 21 registrations outside the US
- Establishments
- 1China
Registered in 2 markets
Where regulators' registries name Shenzhen Baofengtong Electrical Appliances Manufacturing Co. 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 | Shenzhen Baofengtong Electrical Appliances Manufacturing Co. | 1 device types | — | Below |
| Costa Rica | Ministerio de Salud | Manufacturer | Shenzhen Baofengtong Electrical Appliances Manufacturing Co., Ltd. | 1 | — | 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 Shenzhen Baofengtong Electrical Appliances Manufacturing Co. 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 | A6BT-01BT-02BT-03BT-04C101C102C103C260EZ01 28 moreEZ02EZ03EZ04F6Freshening Tablets FT-01HF-10MINIHF-2HF-2 PLUSHF-3HF-3PROHF-5HF-6HF-6 PLUSHF-6EHF-6PHF-7HF-9HF-9PHF-P11HF-P11PLUSHF-P12HV-F007NEREID FRESH 6ORAL IRRIGATIONP11-4SF-02T14Whitening Tablet WT-01 | 2015 |
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 |
|---|---|---|
| SHENZHEN BAOFENGTONG ELECTRICAL APPLIANCES MANUFACTURING CO.,LTDFDA reg. 3011808242 | Shenzhen Guangdong, China | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10050768). 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.