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 13, 2026, FDA's public records list Dunamis with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 14, 2020: Dunamis PunchTac Suture Anchors.
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 |
|---|---|---|
| Feb 14, 2020 | Dunamis PunchTac Suture AnchorsK193245 · MBI | 510(k) clearances |
| Aug 29, 2019 | Dunamis Fixation Button SystemK191319 · MBI | 510(k) clearances |
| Jul 6, 2016 | Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmK160996 · MBI | 510(k) clearances |
| Mar 3, 2016 | Dunamis Force DFX Tensile TapeK153746 · GAT | 510(k) clearances |
| Oct 14, 2015 | Dunamis Interference ScrewK151220 · MBI | 510(k) clearances |
| Jun 29, 2015 | Dunamis Force DFX Suture, Size 5, Dunamis Force DFX Suture Size 2K150327 · GAT | 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
