40 results
·
27ms
·
Sources: EU EUDAMED, US FDA
SCHAEFER WATER CENTER HEMODIALYSIS WATER PURIFICATION SYSTEM, MODEL HWPS-100
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964002685·The ENDO CARRY-ON Procedure Kit contains all of...
Affiniti
FDA UDI
TORNIER, INC.·00846832024612·HUMERAL HEAD TRIAL
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741043697·Catheter Placement Kit
Zavation
FDA UDI
Zavation LLC·00842166183544·GRAFT PADDLE, INFERIOR
MICROPRIME
FDA UDI
Zest Anchors, LLC·00840481135286·MicroPrime G Desensitizer Gel, 1 - 4 mL syringe...
intellijoint HIP®
FDA UDI
Intellijoint Surgical Inc·00628184002490·System, Intellijoint HIP, Portable
Electrode
FDA UDI
I.C. MEDICAL, INC.·00817688020950·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700002490·
NOVABONE-BIOGLASS BONE GRAFT PARTICULATE
FDA 510(k)
FDA Class 2
·Dental
SUNI MAX
FDA 510(k)
FDA Class 1
·Dental
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700002490·
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MNH·June 10, 2016
VERCISE GENUS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·December 23, 2021
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 12, 2013
UNKNOWN DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·February 17, 2011
VOYAGER RX CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·February 14, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·H10·Product code KWP·April 4, 2013
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
Roche brand AccuData GTS Plus System; Catalog number 3000249, material number 03000249001.
FDA Recall
Terminated
·Roche Diagnostics Corp.·Product code CGA·April 18, 2005