Registered with FDA
Double White Medical Technology Development(Guangzhou) Co. L
GUANGZHOU, China. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 10
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Double White Medical Technology Development(Guangzhou) Co. L currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Polishing Agent StripEHM · Class 1 | Polishing & prophylaxis | Lister | Charcoal Teeth Whitening Strips; CVSHealth Brilliant White Whitening Strips(Coconut flavor)CVSHealth Brilliant White Whitening Strips(Peach flavor); Dissolving Teeth Whitening StripsFitreno Teeth Whitening Strips-ONG-YT-01; Teeth Whitening Dry StripsTeeth Whitening Gel Strips; Teeth Whitening Strips,Teeth Whitening U-wraps | 2025 |
| Dental Stain EraserMAU · Class 1 | — | Lister | Charcoal Teeth Whitening Powder; CVS HEALTH TEETH WHITENING PEN; Dentiguard LED Teeth Whitening Kit;EEG Teeth Whitening Kit; Enlight Trading Inc.; Teeth Whitening GelTeeth Whitening Dry Strips, Teeth Whitening Gel Strips, Teeth Whitening U-wraps,Teeth Whitening StripsTeeth Whitening Gel 2ml/ 3ml/ 5ml /10ml; Teeth Whitening Home KitTeeth Whitening Kit; Teeth Whitening Pen; Teeth Whitening Pen-TWP-01Teeth Whitening Powder; Teeth Whitening System | 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 |
|---|---|---|
| DOUBLE WHITE MEDICAL TECHNOLOGY DEVELOPMENT(GUANGZHOU) CO. LTD.FDA reg. 3037591931 | GUANGZHOU Guangdong, China | Foreign exporter |
Other names on FDA records
Double White Medical Technology Development(Guangzhou) Co. Ltd.
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10093182). 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.