Medical Device Manufacturer · US , Woodinville , WA

Lightscalpel, LLC - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2012

Recent clearances: LightScalpel, LIGHT SCALPEL, LIGHTSCALPEL

5
Total
5
Cleared
0
Denied

FDA 510(k) Regulatory Record - Lightscalpel, LLC General & Plastic Surgery ✕

5 devices
1-5 of 5
Cleared Sep 14, 2018
LightScalpel
K173827 · GEX
General & Plastic Surgery · 270d
Cleared Oct 22, 2014
LIGHT SCALPEL
K141658 · GEX
General & Plastic Surgery · 124d
Cleared Jan 02, 2014
LIGHTSCALPEL
K132661 · GEX
General & Plastic Surgery · 129d
Cleared Nov 29, 2012
LIGHTSCALPEL
K123037 · GEX
General & Plastic Surgery · 62d
Cleared Jul 10, 2012
LIGHTSCALPEL FAMILY OF HANDPIECE TIPS FOR CO2 SURGICAL LASERS
K121471 · GEX
General & Plastic Surgery · 53d
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