Manufacturer registered with FDA
Foo Tian Dental Laboratory
Shenzhen, China. Lists 5 dental device types with FDA across 1 registered establishment.
- Device types listed
- 5
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1China
Devices listed with FDA
What Foo Tian Dental Laboratory currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Orthodontic Metal BracketEJF · Class 1 | Orthodontic brackets | Maker | Orthodontic Appliance and customized clear aligners | 2023 |
| Denture Preformed (Partially Prefabricated Denture)EKO · Class 2 | Denture resins & teeth | Maker | Dental Removable Prosthesis like metal dentures&acrylic dentures&valplast denture | 2023 |
| Backing and Facing Artificial TeethELK · Class 1 | — | Maker | Veneers or facings | 2023 |
| Preformed CrownELZ · Class 1 | — | Maker | Fixed Restorations like dental crowns&bridges,post core, inlay or onlay, Zirconia crown or bridge, monolithic Zirconia, | 2023 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | Customized Dental Implant Suprastructure&Substructure | 2023 |
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 |
|---|---|---|
| FOO TIAN DENTAL LABORATORYFDA reg. 3015531834 | Shenzhen Guangdong, China | Foreign exporter, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10060714). 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.