9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
PHOENIX MODELS 250/251 PULSE GENERATORS
FDA 510(k)
FDA Class 3
·Cardiovascular
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668111307·UTRATA CAPSULORRHEXIS FORCEPS TITANIUM
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668106785·UTRATA CAPSULORRHEXIS FORCEPS
PENNINE OXYGEN LINK TUBING
FDA 510(k)
FDA Class 1
·Anesthesiology
IMPLANTABLE PROGRAM-CARDIAC PULSE GEN-OPTIMA MP II
FDA 510(k)
FDA Class 3
·Cardiovascular
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 9, 2014
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012
VANISHPOINT
FDA Adverse Event
Malfunction
·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·September 29, 2010
TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.
FDA Enforcement
Class II
·Terminated·Synthes, Inc.·May 20, 2015