Diagnostics 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 14, 2026, FDA's public records list Beacon Laboratories, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated Mar 11, 1994: FLEXIBLE EXTENDER.
| Mar 11, 1994 | FLEXIBLE EXTENDERK930243 · GEI | 510(k) clearances |
| Jun 25, 1993 | ARGON HANDPIECESK930497 · GEI | 510(k) clearances |
| Apr 20, 1993 | DISPOSABLE ELECTROSURGERY BALL ELECTRODEK925708 · DWG | 510(k) clearances |
| Jan 15, 1993 | SESQUIPOLAR(TM) MIS ELECTRODEK922289 · GEI | 510(k) clearances |
| Dec 24, 1992 | DISPOSABLE HAND-SWITCHING ESU PENCILK925619 · GEI | 510(k) clearances |
| Mar 13, 1992 | MIS ELECTROSURGICAL ELECTRODESK915788 · GEI | 510(k) clearances |
| Feb 3, 1992 | GSU HANDPIECE ADAPTERK920100 · HAM | 510(k) clearances |
| Nov 19, 1991 | PRESSURE GUARDK913772 · HIF | 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
