10 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ULTRADENT PROD RETRACT CORD/ACCESSORY PRODUCT LINE
FDA 510(k)
FDA Class 1
·Dental
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158213692·RETRACTOR JOSEPH NERVE AND WOUND HOOK 1 TOOTH S...
ELMED
FDA UDI
ELMED INCORPORATED·00842180173408·Joseph Skin Hook 6-1/2"
SYNTHES 2.7/3.5MM VARIABLE ANGLE LCP ANKLE TRAUMA SYSTEM-ANTEROLATERAL DISTAL TIBIA PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
MICHEALTH ET 1100/ET 1200 INFARED EAR THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·January 18, 2013
TERUMO STERNAL SAW II
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·December 7, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014
CERVICAL PLATE FIXED SELF-TAPPING SCREW DIAM. 4X18MM (2X)
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KWQ·September 15, 2021
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 12, 2016