Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled 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 Diros Technology with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 27, 2017: OWL RF INSULATED CANNULAE.
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.
| Jun 27, 2017 | OWL RF INSULATED CANNULAEK170708 · GXI | 510(k) clearances |
| Jul 30, 2015 | Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRHK150371 · GXI | 510(k) clearances |
| Dec 30, 2014 | OWL CANNULAEK141586 · GXI | 510(k) clearances |
| Jun 3, 2011 | OWL CANNULAEK102566 · GXI | 510(k) clearances |
| May 5, 2011 | OWL RF PROBESK110593 · GXI | 510(k) clearances |
| Jan 22, 2010 | OWL UNIVERSAL RF SYSTEM URF-3AP (ML)K093185 · GXD | 510(k) clearances |
| Sep 27, 2006 | OWL URF-3APK062758 · GXD | 510(k) clearances |
| Jul 1, 2002 | OWL RADIOFREQUENCY SYSTEM, MODEL URF-2APK021869 · GXD | 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
