7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SUTURE REMOVAL WOUND CLOSURE-INSTRU-
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PMN VOLZ CURETTES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SURE-CUT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 28, 2014
SEE H-10
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·November 15, 2012
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIM·September 14, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015