48 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Vivid S60N / Vivid S70N
FDA 510(k)
FDA Class 2
·Radiology
Comprehensive® SRS
FDA UDI
Biomet Orthopedics, LLC·00880304522725·
PMT® Halo Systems
FDA UDI
PMT CORPORATION·00650551112273·HALO, 1203-5 VEST MEDIUM, LAMBSWOOL LINER, 1211...
Clavicle Plate
FDA UDI
I.T.S. GmbH·09120034304385·Clavicle Plate, 6-Hole
InSePtion MIS Fixation System
FDA UDI
Kalitec Direct LLC·B07314K0112160·Rasp, 16 and 18 mm
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523183821·2 Hole, 16 mm, Right, 1-Level Anterior Cervical...
OSSEOTITE 2 DENTAL IMPLANTS
FDA 510(k)
FDA Class 2
·Dental
PVC FREE INTRAVASCULAR ADMINISTRATION SET
FDA 510(k)
FDA Class 2
·General Hospital
COMPR SRS PROX BDY - SM 48MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWT·September 6, 2013
SYNCHROMED EL
FDA Adverse Event
Death
·RICE CREEK MANUFACTURING·Product code LKK·October 24, 2008
PYXIS ANESTHESIA SYSTEM (PAS)
FDA Adverse Event
Malfunction
·CAREFUSION·Product code BRY·July 12, 2011
RESOLUTION CLIP CLIPPING DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·July 8, 2013
CONSTRAINED GLENOID 22MM LINER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSD·January 31, 2019
TM RVS BASE PLT 25MM POST +2
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·November 25, 2025
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019
MINI REVERSE GLENOID CONST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSD·April 30, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019
NI
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code FTM·March 27, 2020