Lucenxia Prescience AG - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Lucenxia Prescience AG has 9 FDA 510(k) cleared medical devices. Based in Baar, CH.
Historical record: 9 cleared submissions from 2013 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Lucenxia Prescience AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lucenxia Prescience AG
9 devices
Cleared
Apr 30, 2018
Finessis Intense Polyisoprene Surgical Glove
General Hospital
194d
Cleared
Apr 09, 2018
Finessis Zero Flexylon Powder Free Sterile White Surgical Glove Tested for...
General Hospital
161d
Cleared
Oct 20, 2017
Finessis Zero Flexylon Powder Free Sterile White Surgical Glove
General Hospital
109d
Cleared
Feb 08, 2017
Finessis Zero Chemo Flexylon Powder Free Sterile White Surgical Glove
General Hospital
120d
Cleared
Nov 16, 2015
Finessis Corium Flexylon Powder Free Sterile Green Surgical Gloves
General Hospital
154d
Cleared
Nov 16, 2015
Finessis Zero Flexylon Powder Free Sterile White Surgical Glove
General Hospital
154d
Cleared
Sep 25, 2013
FINESSIS VIOLET ELEMENT POLYISOPRENE POWDERFREE STERILE SURGICAL GLOVES
General Hospital
103d
Cleared
May 13, 2013
FINESSIS POLYISOPRENE POWDERFREE SURGICAL GLOVES
General Hospital
171d
Cleared
Mar 18, 2013
STERILE LATEX SURGICAL GLOVE
General Hospital
115d