124 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ZOU ANTERIOR LUMBAR PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARGENCO Au2
FDA UDI
ARGEN CORPORATION, THE·D818121791·Gold based noble metal
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498483·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498384·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498407·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498445·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498360·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498506·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498346·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498421·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498322·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
PINNACLE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295498469·PINNACLE TRI-FLANGE ACETABULAR CUP DUOFIX PATIE...
ROSA SURGICAL DEVICE
FDA 510(k)
FDA Class 2
·Neurology
VERTE-STACK SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CATALYS SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code OOE·March 14, 2016
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020
CATALYS SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code OOE·October 30, 2015
PADGETT MODEL S SLIMLINE ELECTRIC DERMATOME
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code GFD·May 15, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code CAW·September 26, 2014
COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L-TE4BE1AB
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, IRVINE·Product code OAD·May 20, 2011