Medical device makerLabelled 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 Artfx Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 23, 2024: ARTFX Trauma Bone Plate and Screw 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.
| Dec 23, 2024 | ARTFX Trauma Bone Plate and Screw SystemK242939 · HRS | 510(k) clearances |
| Oct 2, 2024 | ARTFX Lumbar PEEK CagesK240889 · MAX | 510(k) clearances |
| Jun 28, 2024 | ARTFX MEDICAL Cervical PEEK CagesK240893 · ODP | 510(k) clearances |
| Apr 20, 2023 | ArtFX Spinal Fixation SystemK212220 · NKB | 510(k) clearances |
| Jun 28, 2022 | Venus Cervical Plate SystemK211718 · KWQ | 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
