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 13, 2026, FDA's public records list Dannik, LLC with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 12, 2025: DANNIK® Laparoscopic Single-Use Poly Specimen Retrieval 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.
| Date | Record | Source |
|---|---|---|
| Mar 12, 2025 | DANNIK® Laparoscopic Single-Use Poly Specimen Retrieval SystemK250411 · GCJ | 510(k) clearances |
| Oct 28, 2021 | Disposable Monopolar Laparoscopic Tips and Reusable HandlesK211019 · GEI | 510(k) clearances |
| Aug 16, 2021 | Disposable Monopolar Laparoscopic Shafts and Reusable HandlesK210569 · GEI | 510(k) clearances |
| Jun 9, 2020 | DANNIK Disposable Monopolar Laparoscopic InstrumentK201063 · GEI | 510(k) clearances |
| Apr 21, 2020 | DANNIK Specimen Retrieval System with deployment mechanism, DANNIK Specimen Retrieval System (Bag Only)K200053 · GCJ | 510(k) clearances |
| Mar 4, 2020 | DANNIK Disposable Monopolar Laparoscopic InstrumentK193019 · GEI | 510(k) clearances |
| Dec 20, 2019 | Dannik Titanium Ligation ClipK192711 · FZP | 510(k) clearances |
| Nov 19, 2019 | Dannik Laparoscopic Suction Irrigation SystemK192643 · GCJ | 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
