Manufacturer registered with FDA
Arctic Biomaterials Oy
Tampere, Finland. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 318 registrations outside the US
- Establishments
- 1Finland
Registered in 3 markets
Where regulators' registries name Arctic Biomaterials Oy 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 | Arctic Biomaterials Oy | 2 device types | — | Below |
| South Korea | MFDS | Manufacturer | Arctic Biomaterials Oy | 16 | 2004–2014 | Pure Global AI |
| Brazil | ANVISA | Manufacturer | ARCTIC BIOMATERIALS OY | 2 | 2003–2021 | 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 Arctic Biomaterials Oy currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Bone PlateJEY · Class 2 | Maxillofacial plates & screws | Maker | — | 2021 |
| Synthetic Bone Grafting MaterialLYC · Class 2 | Bone grafts & membranes | Maker | — | 2022 |
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 |
|---|---|---|
| ARCTIC BIOMATERIALS OYFDA reg. 3015780293 | Tampere Pirkanmaa, Finland | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10062418). 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.