Regent Medical Americas, LLC is one of 23415 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Regent Medical Americas, LLC - FDA 510(k) Cleared Devices
Recent clearances: BIOGEL LATEX POWDER FREE STERILE SURGEON'S GLOVE, BIOGEL SKINSENSE POWDER-FREE NON-LATEX SURGEON'S GLOVE, BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE
7
Total
7
Cleared
0
Denied
Regent Medical Americas, LLC has 7 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 7 cleared submissions from 2005 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Regent Medical Americas, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Regent Medical Americas, LLC
7 devices
Cleared
Apr 10, 2006
BIOGEL LATEX POWDER FREE STERILE SURGEON'S GLOVE
General Hospital
122d
Cleared
Mar 10, 2006
BIOGEL SKINSENSE POWDER-FREE NON-LATEX SURGEON'S GLOVE
General Hospital
126d
Cleared
Mar 07, 2006
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE
General Hospital
88d
Cleared
Feb 01, 2006
BIOGEL ECLIPSE NON-PYROGENIC LATEX POWDER-FREE STERILE SURGEON'S GLOVE
General Hospital
54d
Cleared
Aug 12, 2005
BIOGEL LATEX STERILE POWDER-FREE GLOVE
General Hospital
123d
Cleared
Apr 26, 2005
ECLIPSE LATEX POWDER FREE STERILE SURGEON'S GLOVE
General Hospital
55d
Cleared
Mar 16, 2005
BIOGEL SKINSENSE POLY-ISOPRENE POWDER-FREE NON-LATEX GLOVE
General Hospital
48d