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 Level 1 Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 26, 1996: LEVEL 1 BLOOD STREAM RECOVERY SYSTEM.
| Date | Record | Source |
|---|---|---|
| Apr 26, 1996 | LEVEL 1 BLOOD STREAM RECOVERY SYSTEMK942844 · CAC | 510(k) clearances |
| Jul 12, 1995 | LEVEL 1* INJECT NEEDLE-FREE INJECTION SITEK942271 · FPA | 510(k) clearances |
| May 12, 1994 | PRESSURE IRRIGATING SYSTEMK936223 · GCY | 510(k) clearances |
| Oct 17, 1991 | HOTLINE FLUID WARMERK911383 · LGZ | 510(k) clearances |
| Oct 5, 1987 | LEVEL 1 IR-600 NORMOTHERMIC IRRIGATING SETK873435 · KOD | 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
