16 results · 22ms · Sources: EU EUDAMED, US FDA

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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