Manufacturer registered with FDA
Bonalive Ltd
Turku, Finland. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 12026–2026
- Markets registered in
- 837 registrations outside the US
- Establishments
- 1Finland
510(k) clearances per year, 2007–2026
Registered in 8 markets
Where regulators' registries name Bonalive Ltd 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 | Bonalive Ltd | 1 clearances | 2026–2026 | Below |
| European Union | EUDAMED | Manufacturer | Bonalive Ltd | 19 | — | Pure Global AI |
| Colombia | INVIMA | Registration holder | BONALIVE LTD | 8 | — | Pure Global AI |
| Australia | TGA | Manufacturer | BonAlive Ltd | 4 | 2010–2026 | Pure Global AI |
| Brazil | ANVISA | Manufacturer | BONALIVE LTD | 2 | 2011–2019 | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | Bonalive Ltd | 2 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | BonAlive Ltd | 1 | — | Pure Global AI |
| Peru | DIGEMID | Manufacturer | BONALIVE LTD. | 1 | 2015–2015 | 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 Bonalive Ltd currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Synthetic Bone Grafting MaterialLYC · Class 2 | Bone grafts & membranes | Maker | Bonalive Maxillofacial | 2026 |
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 |
|---|---|---|
| BONALIVE LTDFDA reg. 3008328709 | Turku Varsinais-Suomi, Finland | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10031930). 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.