Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of OlympusLabelled by claude-sonnet-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 Somnus Medical Technologies with 16 510(k) clearances. The most recent is a 510(k) clearance dated May 30, 2000: SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLE.
| May 30, 2000 | SOMNUS DISPOSABLE TISSUE COAGULATING ELECTRODE AND SOMNUS REUSABLE CONNECTOR CABLEK000720 · GEI | 510(k) clearances |
| May 16, 2000 | SOMNUS MODEL S2 ELECTROSURGICAL GENERATORK001438 · GEI | 510(k) clearances |
| Mar 17, 2000 | ELECTROSURGICAL GENERATOR, MODEL S1K000501 · GEI | 510(k) clearances |
| Nov 2, 1998 | SOMNOPLASTY SYSTEM, MODELS S2, 1010/2010,2000/1000,1100,3000/30XX/6000, 1200K982717 · GEI | 510(k) clearances |
| Jan 30, 1998 | SOMNUS TISSUE COAGULATING ELECTRODEK973701 · GEI | 510(k) clearances |
| Jan 9, 1998 | SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODEK970837 · GEI | 510(k) clearances |
| Jan 9, 1998 | SOMNUS MODEL 30XX DISPOSABLE TRI-NEEDLE COAGULATING ELECTRODEK970838 · GEI | 510(k) clearances |
| Dec 19, 1997 | SOMNOPLASTY SYSTEMK973618 · GEI | 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
