Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of StrykerLabelled 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 14, 2026, FDA's public records list Wrightmedicaltechnologyinc with 302 510(k) clearances. The most recent is a 510(k) clearance dated Jan 27, 2023: Prophecy Preoperative Navigation Alignment System.
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.
| Jan 27, 2023 | Prophecy Preoperative Navigation Alignment SystemK222835 · HSN | 510(k) clearances |
| Jan 5, 2022 | PRO-DENSE LoVisc Bone Graft SubstituteK213342 · MQV | 510(k) clearances |
| Nov 16, 2021 | Sterile PHALINX Hammertoe SystemK212996 · HWC | 510(k) clearances |
| Mar 10, 2021 | PROPHECY Preoperative Navigation Alignment SystemK202815 · HSN | 510(k) clearances |
| Jan 8, 2021 | ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating SystemK201259 · HRS | 510(k) clearances |
| Oct 21, 2020 | PRO-DENSE LoVisc Bone Graft SubstituteK200507 · MQV | 510(k) clearances |
| Jun 8, 2020 | The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total Ankle Revision SystemK193067 · HSN | 510(k) clearances |
| Aug 22, 2019 | INFINITY Total Ankle System, INBONE Total Ankle SystemK191393 · HSN | 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
