22 results · 20ms · Sources: EU EUDAMED, 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