Registered with FDA
Diversity Corporation FZE
Sharjah, United Arab Emirates. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 24 registrations outside the US
- Establishments
- 1United Arab Emirates
Registered in 2 markets
Where regulators' registries name Diversity Corporation FZE as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Lister | Diversity Corporation FZE | 3 device types | — | Below |
| South Korea | MFDS | Manufacturer | DIVERSITY CORPORATION FZE.DIVERSITY CORPORATION FZE | 4 | 2014–2014 | 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 Diversity Corporation FZE currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Surgical Tooth Extractor ForcepsEMG · Class 1 | Dental hand instruments | Lister | Forceps | 2024 |
| Surgical Rongeur ForcepsEMH · Class 1 | Dental hand instruments | Lister | Surgical | 2023 |
| Orthodontic PlierJEX · Class 1 | Dental hand instruments | Lister | Plier | 2024 |
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 |
|---|---|---|
| DIVERSITY CORPORATION FZEFDA reg. 3009718267 | Sharjah Ash Shariqah, United Arab Emirates | Foreign exporter |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10052025). 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.