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 14, 2026, FDA's public records list Hommed, LLC with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 18, 2004: HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS.
| Aug 18, 2004 | HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONSK040799 · DXN | 510(k) clearances |
| Aug 10, 2004 | HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEMK040651 · DXN | 510(k) clearances |
| Feb 27, 2004 | CENTRAL STATION, VERSION 3.3HK040032 · DXN | 510(k) clearances |
| Apr 22, 2002 | HOMMED CENTRAL STATIONK020184 · DXN | 510(k) clearances |
| Apr 9, 2002 | HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READERK014025 · DQA | 510(k) clearances |
| Jun 28, 2001 | HOMMED OBSERVER, MODEL IK003180 · DXN | 510(k) clearances |
| Mar 2, 2001 | HOMMED SENTRY III PATIENT MONITOR SYSTEMK004044 · DQA | 510(k) clearances |
| Mar 15, 2000 | THE HOMMED SENTRY, MODEL 1 SENTRYK993938 · DXN | 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
