Manufacturer registered with FDA
Larident SRL
TRIBOGNA, Italy. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 529 registrations outside the US
- Establishments
- 1Italy
Registered in 5 markets
Where regulators' registries name Larident SRL 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 | Larident SRL | 4 device types | — | Below |
| European Union | EUDAMED | Manufacturer | Larident SRL | 15 | — | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | Larident S.R.L | 10 | — | Pure Global AI |
| Australia | TGA | Manufacturer | Larident SRL | 2 | 2006–2009 | Pure Global AI |
| Israel | AMAR | Manufacturer | LARIDENT SRLLarident SRL | 2 | — | 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 Larident SRL currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Saliva Ejector MouthpieceDYN · Class 1 | — | Maker | Cannula Zero Saliva Ejector | 2024 |
| Dental Hand InstrumentsDZN · Class 1 | Dental hand instruments | Maker | DEL JECT AMALGAM GUN | 2011 |
| Roll CottonEFN · Class 1 | — | Maker | Cotton Roll Holder | 2024 |
| Dental Plastic Filling InstrumentEIY · Class 1 | Dental hand instruments | Maker | IMPLA-CLEAN | 1994 |
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 |
|---|---|---|
| LARIDENT S.R.L.FDA reg. 9680507 | TRIBOGNA Genova, Italy | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9009559). 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.