16 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Keos Anterior Cervical Interbody Fusion Device System
FDA 510(k)
FDA Class 2
·Orthopedic
D-LISH
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·00302730002188·Young D-Lish 5% Sodium Fluoride Varnish, 0.40mL...
D-Lish Fresh Melon Varnish 50
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·10302732124502·
GII ETHIBOND
FDA UDI
DEPUY MITEK, LLC·10886705002061·Arthroscopic GII EasyAnchor Size 2 (5 metric) g...
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78821245000101·EXPERIENCE Mini ROTH 022/LR5-22T-1A 4D
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78821245000201·EXPERIENCE Mini MBT 022/LR5-17T 2A
MHI-TM2000 LINEAR ACCELERATOR SYSTEM VERO IMAVIS
FDA 510(k)
FDA Class 2
·Radiology
DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX¿ SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·September 22, 2021
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 23, 2024
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 30, 2014
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·March 9, 2007
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 9, 2013
SMR CEMENTLESS FINNED STEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HSD·August 28, 2023
GII EASY ARTHRO #2 ETH *EA
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code JDR·January 23, 2019
DRX Revolution Mobile X-Ray System
FDA Enforcement
Class II
·Ongoing·Carestream Health, Inc.·December 13, 2023