ClearanceBrief
Company ยท US

Usa Laser Biotech, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2016. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ILYLamp, Infrared, Therapeutic Heating6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 26, 2016K161198Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3
Usa Laser Biotech, Inc.
ILY
Jul 5, 2016K160947LUMIX 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
Usa Laser Biotech, Inc.
ILY
Feb 17, 2011K101893NEXUS BIOWAVE 7W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 10W LITE IR LAMP SYSTEM, NEXUS BIOWAVE 30W PRO IR LAMP SYSTEM, NEXUS
Usa Laser Biotech, Inc.
ILY
Oct 28, 2009K091726NEXUS XPULSE 805 IR LAMP SYSTEM, NEXUS XPULSE 980 IR LAMP SYSTEM, MODEL 805, 980
Usa Laser Biotech, Inc.
ILY
Nov 30, 2005K052814LUMINA 1600, 3300 AND 6600 SYSTEMS
Usa Laser Biotech, Inc.
ILY
Nov 17, 2004K042256IR HEAT LAMP SYSTEMS: ICL 15 HFPL SYSTEM, ICL 60 PLUS HFPL SYSTEM (MODELS 40, 100 AND 250), ICL 100 ACTIVO SCANNER SYSTE
Usa Laser Biotech, Inc.
ILY

Latest recalls

DateFirm and productCodeLinked 510(k)
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