Nutra Luxe MD, LLC is one of 4740 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nutra Luxe MD, LLC - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Nutra Luxe MD, LLC has 9 FDA 510(k) cleared medical devices. Based in Sparks, US.
Historical record: 9 cleared submissions from 2014 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Nutra Luxe MD, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nutra Luxe MD, LLC
9 devices
Cleared
Dec 15, 2016
Pulsaderm ACE-All Blue
General & Plastic Surgery
113d
Cleared
Oct 19, 2016
Pulsaderm Acne Device
General & Plastic Surgery
96d
Cleared
Sep 16, 2016
NutraStim Hair Laser Helmet
General & Plastic Surgery
184d
Cleared
Feb 10, 2016
Nutra Face Lift Model PE8050
Neurology
317d
Cleared
Jul 22, 2015
Nutra Light Advanced
General & Plastic Surgery
159d
Cleared
Jan 08, 2015
NUTRA STIM HAIR LASER COMB
General & Plastic Surgery
209d
Cleared
Jan 08, 2015
NUTRA STIM HAIR LASER COMB
General & Plastic Surgery
209d
Cleared
Aug 20, 2014
NUTRA LIGHT RED
General & Plastic Surgery
93d
Cleared
May 23, 2014
NUTRA LIGHT BLUE
General & Plastic Surgery
255d