Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Dentsply SironaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Astra Tech with 38 510(k) clearances. The most recent is a 510(k) clearance dated Jan 23, 2013: OSSEOSPEED ANGLED ABUTMENT EV.
| Jan 23, 2013 | OSSEOSPEED ANGLED ABUTMENT EVK121810 · NHA | 510(k) clearances |
| Oct 31, 2012 | LOFRIC PRIMO, LOFRIC HYDRO-KITK122078 · EZD | 510(k) clearances |
| Jul 31, 2012 | OSSEOSPEED PLUSK120414 · DZE | 510(k) clearances |
| Jul 5, 2012 | ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIAK120338 · NHA | 510(k) clearances |
| Apr 17, 2012 | LOFRIC SINGLE USE URINARY CATHETERK113424 · EZD | 510(k) clearances |
| Mar 1, 2012 | ATLANTIS(TM) ABUTMENT AND ATLANTIS(TM) CROWN ABUTMENT FOR KEYSTONE GENESIS IMPLANT, ATLANTIS GEMINI(TM) ABUTMENT...K113003 · NHA | 510(k) clearances |
| Dec 1, 2011 | ATLANTIS ABUTMENT IN ZIRCONIA FOR ASTRA TECH OSSEOSPEED PLUS IMPLANTK112138 · NHA | 510(k) clearances |
| Sep 26, 2011 | ASTRA TECH IMPLANT SYSTEMK111287 · DZE | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
