Medical device makerLabelled 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 15, 2026, FDA's public records list Aptis Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 3, 2019: Aptis Medical Distal Radio Ulnar Joint Implant.
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.
| May 3, 2019 | Aptis Medical Distal Radio Ulnar Joint ImplantK190599 · KXE | 510(k) clearances |
| Apr 3, 2015 | Aptis Medical Distal Radio Ulnar Joint ImplantK142569 · KXE | 510(k) clearances |
| Oct 24, 2008 | DISTAL RADIO-ULNAR JOINT IMPLANTK082839 · KXE | 510(k) clearances |
| Dec 7, 2005 | DISTAL RADIO-ULNAR JOINT IMPLANTK053119 · KXE | 510(k) clearances |
| Jan 26, 2005 | DISTAL RADIO-ULNAR JOINT IMPLANTK040497 · KXE | 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
