Data / Medical devices / Implant, Endosseous, Root-Form / Sweden
FDA-registered makers of Implant, Endosseous, Root-Form in Sweden: 7 establishments
7 establishments in Sweden are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Implant, Endosseous, Root-Form
- Product code
- DZE
- Country
- Sweden
Makers of Implant, Endosseous, Root-Form in Sweden
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Nobel Biocare AB | GOTEBORG Vastra Gotaland, Sweden | Specification developer | 31 | February 18, 2026 | 0 | 2 | 0 | api.fda.gov |
| Dentsply IH AB | MOLNDAL Vastra Gotaland, Sweden | Manufacturer, Specification developer | 30 | November 16, 2022 | 0 | 0 | 0 | api.fda.gov |
| Neoss AB | Goteborg Vastra Gotaland, Sweden | Manufacturer | 4 | September 5, 2012 | 0 | 0 | 0 | api.fda.gov |
| Dentatus AB | SPANGA Stockholm, Sweden | Manufacturer | 1 | September 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| Nobel Biocare AB, Produktion | KARLSKOGA Orebro, Sweden | Contract manufacturer, Manufacturer | 1 | February 18, 2026 | 0 | 0 | 0 | api.fda.gov |
| Cenova AB | MJOLBY Ostergotland, Sweden | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Elos Medtech Timmersdala AB | TIMMERSDALA Vastra Gotaland, Sweden | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.