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 Solaris Medical Technology, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 7, 2010: NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103.
| Oct 7, 2010 | NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103K100077 · DQA | 510(k) clearances |
| Jul 22, 2010 | SOLARIS REUSABLE AND DISPOSABLE BLOOD PRESSURE CUFFSK101972 · DXQ | 510(k) clearances |
| Mar 12, 2010 | SOLARIS MODELS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIESK092950 · DQA | 510(k) clearances |
| Jul 25, 2008 | SOLARIS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIESK073249 · DQA | 510(k) clearances |
| Jan 31, 2007 | SOLARIS COMPATIBLE REUSABLE ADULT SPO2 FINGER SENSORS, MODELS S100A-090103 AND 300103, S200A-090101 AND 300101K061931 · DQA | 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
