Wellquest Intl., Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wellquest Intl., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Wellquest Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 1997 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wellquest Intl., Inc. Filter by specialty or product code using the sidebar.
Wellquest Intl., Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Aug 17, 2014
NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE
General & Plastic Surgery
370d
Cleared
Dec 17, 1997
DAPELLE HAIR REMOVER
General & Plastic Surgery
76d