Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Osartis GmbH with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 20, 2024: Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 20, 2024 | Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer MoldsK240856 · MBB | 510(k) clearances |
| May 18, 2021 | BonOs Inject, Pedicle screw kits, Cement pusherK202458 · LOD | 510(k) clearances |
| Mar 19, 2021 | BonOs HV, BonOs MV, BonOs LVK210120 · LOD | 510(k) clearances |
| Mar 19, 2021 | BonOs HV Genta, BonOs MV Genta, BonOs LV GentaK210125 · LOD | 510(k) clearances |
| Dec 2, 2019 | Hi-Fatigue Bone CementK192394 · LOD | 510(k) clearances |
| Nov 27, 2019 | Hi-Fatigue G Bone CementK192379 · LOD | 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
