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 USA Laser Biotech with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 26, 2016: Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3.
| Jul 26, 2016 | Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3K161198 · ILY | 510(k) clearances |
| Jul 5, 2016 | LUMIX CPS 1 IR Lamp System LUMIX CPS 2 IR Lamp System LUMIX CPS 3 IR Lamp System LUMIX CPS 4 IR Lamp System LUMIX CPS 5 IR Lamp SystemK160947 · ILY | 510(k) clearances |
| Feb 17, 2011 | NEXUS BIOWAVE 7W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 10W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 30W PRO IR LAMP SYSTEM, NEXUSK101893 · ILY | 510(k) clearances |
| Oct 28, 2009 | NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980K091726 · ILY | 510(k) clearances |
| Nov 30, 2005 | LUMINA 1600, 3300 AND 6600 SYSTEMSK052814 · ILY | 510(k) clearances |
| Nov 17, 2004 | IR HEAT LAMP SYSTEMS: ICL 15 HFPL SYSTEM, ICL 60 PLUS HFPL SYSTEM (MODELS 40, 100 AND 250), ICL 100 ACTIVO SCANNER SYSTEK042256 · ILY | 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
