16 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MAYFIELD INFINITY XR2 SKULL CLAMP, MODEL A-2114
FDA 510(k)
FDA Class 2
·Neurology
LEONE SPA
FDA UDI
LEONE SPA·08033707065777·INTRAORAL ELASTICS 6,5 oz 1/8" brown
LEONE SPA
FDA UDI
LEONE SPA·08033707065678·INTRAORAL ELASTICS 2,5 oz 3/8" orange
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0105060·Inserter Sleeve, All Size Implants
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345024243·Lumbar Inserter, Inline- Lateral
Phonak
FDA UDI
Phonak AG·07612847867987·Phonak Ambra microM (black)
BIO-FASTAK SUTURE ANCHOR, MODEL AR-1324B
FDA 510(k)
FDA Class 2
·Orthopedic
MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS WITH CEFTRIAXONE (0.5-128 UG/ML)
FDA 510(k)
FDA Class 2
·Microbiology
BD VACUTAINER® SODIUM FLUORIDE POTASSIUM OXALATE (FX) BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·April 19, 2018
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 17, 2025
INFANT BREATHING CIRCUIT FOR SLE 2000/2000HFO
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·September 7, 2009
TENDRIL ST
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·May 2, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 15, 2014
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 26, 2011
HEARTMATE II LEFT VENTRICULAR ASSIST SYSTEM, NA
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 15, 2019
Medtronic Model 37711 Restore Neurostimulator. The Restore Neurostimulator is an implanted, rechargeable neurostimulator which provides pain management therapy.
FDA Recall
Terminated
·Medtronic Inc, Neurological & Spinal Division·Product code GZB·November 22, 2005