19 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SEE-IT CARIES DETECTOR
FDA 510(k)
FDA Class 2
·Dental
CTXA Hip Extended Reference Data
FDA UDI
MINDWAYS SOFTWARE, INC.·B052DICTXAHIPEXTDB0·The CTXA Hip Extended Reference Data is an acce...
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70603301·Mini-Mono-Brackets Roth 'N' .018" 9° 400 Bracke...
Klitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0603500·Tray, Base, 3.5"
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306813542·Jeweler Forceps, 45° Tip, 11cm
VANGUARD COMPLETE KNEE CRUCIATE RETAINING POROUS & HA FEMUR LEFT 75MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code MBH·December 16, 2016
ARROW REDIGUARD, 9FR. 50CC, INTRA-AORTIC BALLOON VATHETER, IAB-R950-U
FDA 510(k)
FDA Class 2
·Cardiovascular
NITRILE PATIENT EXAMINATION GLOVE (GREEN COLOR), POWDER FREE, NON STERILE
FDA 510(k)
FDA Class 1
·General Hospital
Widex
FDA UDI
Widex A/S·05706069673500·Widex EVOKE E-CIC TR (Light beige ) 330, Right,...
Widex
FDA UDI
Widex A/S·05706069673524·Widex EVOKE E-CIC TR (Dark brown ) 330, Right, ...
Widex
FDA UDI
Widex A/S·05706069673517·Widex EVOKE E-CIC TR (Clay brown ) 330, Right, ...
Truliant CC
FDA UDI
Exactech, Inc.·10885862612458·TRULIANT CC FEMORAL SIZE 3, RIGHT
Optetrak Logic
FDA UDI
Exactech, Inc.·10885862265715·
CONFIDENCE KIT, NO NEEDLES
FDA Adverse Event
Malfunction
·DEPUY SYNTHES SPINE·Product code NDN·April 1, 2014
ACUVUE OASYS BRAND CONTACT LENSES
FDA Adverse Event
Injury
·VISTAKON·Product code LPM·April 11, 2013
ONE TOUCH ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·June 13, 2008
ACCESS® 2 IMMUNOASSAY CLINICAL SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·April 15, 2011
ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·August 29, 2019
NON-STERILE KIRSCHNER WIRES AND STEINMANN PINS, MODELS #'S 290-101/160, 290-201/216, 290-060/330, 290-161/220
FDA 510(k)
FDA Class 2
·Orthopedic