22 results
·
48ms
·
Sources: EU EUDAMED, US FDA
PGD-PRE-IMPLANTATION GENETIC DIAGNOSTIC PIPETTES (BIOPSY PIPETTES)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Bard® Nelaton Catheters
FDA UDI
C. R. Bard, Inc.·10801741122559·Bard® Nelaton Catheters
CORTICAL LOCKING SCREW 3.5mm x 16mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665007824·
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613059279·Tissue Forceps, 4 x 5 Teeth, Overall Length 6-1/4"
N/A
FDA UDI
TETRA MEDICAL SUPPLY CORP.·00614138101739·PREMIUM POLYESTER LATEX FREE ELASTIC BANDAGE 6I...
#014160-TAB TUBING ROTATOR ADAPTOR
FDA 510(k)
FDA Class 2
·Cardiovascular
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·February 12, 2026
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567654·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567685·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567678·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567708·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567692·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033567661·
ACTIVA PC
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·September 12, 2011
E-Z EM PERCUPUMP 2001 CT INJECTOR
FDA 510(k)
FDA Class 2
·Radiology
WILLI GELLER CREAPEARL
FDA 510(k)
FDA Class 2
·Dental
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
TENDRIL ST
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
BONE SCREW SELF-TAPPING 6.5 MM DIA. 30 MM LENGTH
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025