7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
TUBING, FLEXIBLE, MEDICAL GAS
FDA 510(k)
FDA Class 1
·Anesthesiology
Sapphire Dorsal Comfort Fit
FDA 510(k)
FDA Class 2
·Dental
PALOMAR ASPIRE LASER PLATFORM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNKNOWN DEPUY TIBIAL INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·April 30, 2014
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·October 10, 2012
CONQUEST PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·April 15, 2015
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
FDA Enforcement
Class II
·Terminated·CryoLife, Inc.·July 19, 2017