118 results
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29ms
·
Sources: EU EUDAMED, US FDA
BABY TEETHER, MODEL 20104
FDA 510(k)
FDA Class 2
·Dental
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00140231·
Versacryl
FDA UDI
Keystone Industries·H66810140231·Acrylic Pink 1 lb Pwd
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554432·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554456·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554470·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554449·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554463·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033554425·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100230·SNII Awl Tap, 7.50mm
Matira
FDA UDI
Kalitec Direct LLC·B07307K0100230·Assembly, Caddie, 4L Plates, Hinged
D.SIGN 96
FDA 510(k)
FDA Class 2
·Dental
INTRA OPERATIVE RADIATION THERAPY
FDA 510(k)
FDA Class 2
·Radiology
ELLUME COVID-19 HOME TEST
FDA Adverse Event
Malfunction
·ELLUME LIMITED·Product code QKP·December 20, 2021
BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 22, 2021
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
INJECTION NEEDLE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·March 10, 2011
ADVIA CENTAUR
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS MFG LTD·Product code MMI·March 14, 2008
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026