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 13, 2026, FDA's public records list Allmed Systems, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 18, 2014: SPHINX JR.
| Mar 18, 2014 | SPHINX JRK132975 · GEX | 510(k) clearances |
| Feb 19, 2013 | REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200K110941 · GEX | 510(k) clearances |
| Jun 21, 2007 | FLEXGUARDK070924 · GEX | 510(k) clearances |
| Apr 17, 2007 | REVOLIX DUO LASER SYSTEMK070466 · GEX | 510(k) clearances |
| Mar 26, 2007 | REVOLIX 120K070476 · GEX | 510(k) clearances |
| Jun 1, 2005 | REVOLIX AND REVOLIX JRK051167 · GEX | 510(k) clearances |
| Jan 20, 2004 | SPHINX LASER SYSTEMSK033437 · GEX | 510(k) clearances |
| Jan 15, 2004 | REVOLIX LASER SYSTEMSK033423 · 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
