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 Omnitech Systems, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 27, 2016: Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode.
| Date | Record | Source |
|---|---|---|
| Jun 27, 2016 | Omnitech HF Resection Electrodes, Omnitech HF Vaporization ElectrodeK151976 · FAS | 510(k) clearances |
| May 27, 2005 | OMNITECH FULGURATING ELECTRODEK050454 · FAS | 510(k) clearances |
| Jul 17, 1998 | OMNITECH RESECTOSCOPE ROLLER ELECTRODEK981463 · KNF | 510(k) clearances |
| Jul 10, 1998 | OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODEK981464 · KNF | 510(k) clearances |
| Apr 22, 1997 | RESECTOSCOPE CUTTING LOOP ELECTRODEK964365 · FAS | 510(k) clearances |
| Mar 19, 1997 | OMNITECH RESECTOSCOPE ROLLER ELECTRODEK965093 · FAS | 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
