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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Clinicon with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 2012: SURELASE CO2 LASER SYSTEM.
| Date | Record | Source |
|---|---|---|
| Sep 25, 2012 | SURELASE CO2 LASER SYSTEMK121580 · GEX | 510(k) clearances |
| Mar 2, 2007 | CO2 LASER SYSTEM, MODEL C-LASK063698 · GEX | 510(k) clearances |
| Mar 26, 2002 | CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIESK014236 · GEX | 510(k) clearances |
| Feb 11, 2002 | CLINICON UNIVERSAL WAVEGUIDE HANDPIECE AND FIBER TIPSK014048 · GEX | 510(k) clearances |
| Sep 8, 1999 | SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEMK992472 · GEX | 510(k) clearances |
| Dec 11, 1998 | SURECAUT DIAMOND LASER KNIFEK983463 · GEX | 510(k) clearances |
| Oct 29, 1997 | C4K970143 · GEX | 510(k) clearances |
| Aug 8, 1997 | SURESCANK964831 · GEX | 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
