15 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BENZ 38 CLEAR & WITH BLUE VISIBILITY TINT
FDA 510(k)
FDA Class 2
·Ophthalmic
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295234913·P.F.C. SIGMA OVAL-DOME PATELLA 3-PEG TRIAL 41mm
Novo Surgical Inc.
FDA UDI
NOVO SURGICAL, INC.·00842331155369·thermoplastic instrument tray, micro tray for s...
HAEMONETICS 40U RBC FILTER BAG
FDA 510(k)
FDA Class 2
·General Hospital
US SA Implant System
FDA 510(k)
FDA Class 2
·Dental
MERIT HEMOSTASIS VALVE
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DQX·August 25, 2011
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·January 30, 2013
SYNERGY
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·January 12, 2011
EON MINI
FDA Adverse Event
Injury
·ST JUDE MEDICAL NEUROMODULATION·Product code GZB·July 15, 2014
AIA-900
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·February 24, 2016
E1 RINGLOC ACETEABULAR LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWL·May 17, 2017
TOSOH AIA-900
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·December 13, 2016
A1A-600II
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·October 28, 2016
TOSOH AIA-1800
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·November 11, 2016
AIA-360
FDA Adverse Event
Injury
·TOSOH CORPORATION·Product code KHO·March 3, 2016