Innovaquartz, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Innovaquartz, LLC - FDA 510(k) Cleared Devices
Recent clearances: VaporMAX LDD, ProFlex CO2 Laser Fiber, ProFlex Laser Fibers
4
Total
4
Cleared
0
Denied
Innovaquartz, LLC has 4 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Latest FDA clearance: May 2024. Active since 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innovaquartz, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innovaquartz, LLC
4 devices
Cleared
May 03, 2024
VaporMAX LDD
General & Plastic Surgery
219d
Cleared
Sep 20, 2021
ProFlex CO2 Laser Fiber
General & Plastic Surgery
266d
Cleared
Apr 20, 2018
ProFlex Laser Fibers
General & Plastic Surgery
92d
Cleared
Dec 19, 2014
ProFlex Laser Fibers (ProFlex 200) and ProFlex Laser Fibers (PRoFlex 273)
General & Plastic Surgery
93d