Global USA Distribution, LLC is one of 21644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Global USA Distribution, LLC - FDA 510(k) Cleared Devices
Recent clearances: SKINCLEAR Q-SWITCHED ND:YAG LASER, LASERPEEL SOFT-MET MODIFIED ERBIUM LASER, NANNOLIGHT INTENSE PULSED LIGHT SYSTEM
4
Total
4
Cleared
0
Denied
Global USA Distribution, LLC has 4 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Historical record: 4 cleared submissions from 2008 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Global USA Distribution, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Global USA Distribution, LLC
4 devices
Cleared
Dec 16, 2008
SKINCLEAR Q-SWITCHED ND:YAG LASER
General & Plastic Surgery
40d
Cleared
Aug 08, 2008
LASERPEEL SOFT-MET MODIFIED ERBIUM LASER
General & Plastic Surgery
22d
Cleared
Jul 31, 2008
NANNOLIGHT INTENSE PULSED LIGHT SYSTEM
General & Plastic Surgery
14d
Cleared
Apr 07, 2008
SKIN CLEAR SRVH LONG-PULSED ND: YAG LASER
General & Plastic Surgery
26d