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 15, 2026, FDA's public records list Sandstone Medical Technologies, LLC with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jul 18, 2012: POLARIS Q-SWITCH RUBY SYSTEM.
| Jul 18, 2012 | POLARIS Q-SWITCH RUBY SYSTEMK121162 · GEX | 510(k) clearances |
| Jul 1, 2011 | CORTEX CO2 / ER:YAG LASER SYSTEMK110897 · GEX | 510(k) clearances |
| Apr 27, 2011 | TRIPLEX ER. YAG / ND: YAG SYSTEMK110502 · GEX | 510(k) clearances |
| Apr 8, 2011 | APEX ER. YAG / IPL SYSTEMK110304 · GEX | 510(k) clearances |
| Jun 16, 2010 | CHEVEUX DIODE LASER SYSTEMK100893 · GEX | 510(k) clearances |
| Feb 18, 2010 | LS-40 CO2 LASER SYSTEM MODEL LS-40K093793 · GEX | 510(k) clearances |
| Feb 3, 2009 | MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEMK082407 · GEX | 510(k) clearances |
| Nov 5, 2008 | LS FAMILY OF CO2 LASERS WITH SCANNING HANDPIECEK082101 · 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
