• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
1 to 10 of 63 Results
ProductCode: GEX Applicant: LUMENIS Decision Date To: 07/29/2015
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
Results per Page
New Search  
Export all 63 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
ultrapulse alpha co2 laser system, delivery devices and accessories Lumenis Be Ltd. K233301 12/01/2023
lumenis y&r laser system Lumenis Inc. K211979 06/21/2022
the family of ultrapulse co2 surgical and aesthetic lasers, delivery devices and accessories Lumenis Be, Ltd. K220467 05/18/2022
acupulse co2 laser system, delivery devices and accessories Lumenis, Ltd. K212703 10/19/2021
ultrapulse surgical and aesthetic co2 laser system, delivery devices and accessories Lumenis Ltd. K203544 12/24/2020
acupulse w co2 laser systems, delivery devices and accessories Lumenis Ltd. K202428 10/22/2020
acupulse w co2 laser systems, delivery devices and accessories Lumenis Ltd. K201663 07/16/2020
stellar m22 for intense pulsed light (ipl) and laser system Lumenis Ltd. K193500 01/16/2020
acupulse (previously called acupulse 30/40 st); acupulse 40w g; acupulse duo Lumenis Ltd. K180597 04/03/2018
lightsheer desire; lightsheer desire light; lightsheer duet; lightsheer infinity Lumenis Ltd. K170179 09/18/2017
-
-