Usa Laser Biotech, Inc. is one of 18376 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Usa Laser Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3, 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 System, NEXUS 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. has 6 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 6 cleared submissions from 2004 to 2016. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Usa Laser Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Texas Applied Biomedical Services, Inc. as regulatory consultant.