22 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATLAS IMPLANT SYSTEM - WIDE PLUS
FDA 510(k)
FDA Class 2
·Dental
TruForm
FDA UDI
Rmo, Inc.·00885797099594·MAN 1ST MOLAR LEFT 87 BANDS
ELMED
FDA UDI
ELMED INCORPORATED·00842180184169·BITE BLOCK, MOUTH PROP, BLACK, SMALL
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613120641·Bite Block, Mouth Prop, Small *********
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036026677·
RocaFlow - Irrigation, Warming and Suction System - Double Chamber
FDA UDI
Promepla·03700512955252·with Aspiration Pump
FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN
FDA 510(k)
FDA Unclassified
·Unknown
GUTHRIE SHIELD BLUE LATEX EXAMINATION GLOVES, POWDERED WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
COPPERHEAD CERVICAL INTERBODY CAGE
FDA Adverse Event
Injury
·EMINENT SPINE·Product code ODP·January 8, 2016
TGS UKA SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014
BD POSIFLUSH¿ NORMAL SALINE SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 30, 2023
TGS UKA SYSTEM
FDA Adverse Event
Injury
·CAYENNE MEDICAL INC.·Product code HSX·May 15, 2014
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013
TGS UKA KNEE SYSTEM
FDA Adverse Event
Injury
·ALEXANDRIA RESEARCH TECHNOLOGIES, LLC·Product code HSX·August 14, 2013
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·April 19, 2013
PANORAMA CENTRAL STATION WITH TELEMETRY
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code MHX·August 18, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 11, 2011