48 results
·
20ms
·
Sources: EU EUDAMED, US FDA
NUVASIVE CEMENT RESTRICTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Baltic Denture System BD Load
FDA UDI
Merz Dental GmbH·D7091032180·Baltic Denture System BDLoad Ln6 PLSEbil2DFl A2...
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120321801·Diamond, pointed, COOL DIAMANT, medium grit
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197470940·Lucae tympanum perforator
18 cm,...
SIMPLICITY DISPOSABLE PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
A-WEAR
FDA 510(k)
FDA Class 2
·Dental
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
ULTRA DRIVE 6MM PLUG PULLER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDX·July 20, 2022
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445527·The HOTWIRE™ is a sterile, single-use guidewire...
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445503·The HOTWIRE™ is a sterile, single-use guidewire...
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445510·The HOTWIRE™ is a sterile, single-use guidewire...
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·November 28, 2019
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·January 6, 2021
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·May 22, 2018
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·April 3, 2013
PALMAZ GENESIS OPTA PRO
FDA Adverse Event
Injury
·CORDIS EUROPA, N.V.·Product code FGE·March 29, 2011
SWAN-GANZ CONTINUOUS CARDIAC OUTPUT CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DYG·April 16, 2008