Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 13, 2026, FDA's public records list Neoss with 10 510(k) clearances. The most recent is a 510(k) clearance dated May 17, 2022: Neoss Individual Prosthetics.
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.
| Date | Record | Source |
|---|---|---|
| May 17, 2022 | Neoss Individual ProstheticsK211396 · NHA | 510(k) clearances |
| Oct 5, 2020 | Membrane Screws and Membrane TacksK201561 · DZL | 510(k) clearances |
| Oct 8, 2015 | Neoss TiBase, Neoss CoCr Abutments (Mono and Multi)K150669 · NHA | 510(k) clearances |
| Apr 13, 2015 | Neoss Ti Reinforced MembraneK143327 · NPK | 510(k) clearances |
| Sep 5, 2012 | NEOSS PROACTIVE TAPERED IMPLANTK113376 · DZE | 510(k) clearances |
| May 22, 2009 | NEOSS IMPLANT SYSTEM 03.25K090452 · DZE | 510(k) clearances |
| Mar 2, 2009 | NEOSS ACCESS ABUTMENTSK081851 · NHA | 510(k) clearances |
| Feb 11, 2009 | NEOSS PROACTIVE IMPLANTK083561 · 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
