28 results
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20ms
·
Sources: EU EUDAMED, US FDA
NovoPen Echo
FDA 510(k)
FDA Class 2
·General Hospital
ANSWER HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304005365·
Mouthpiece, Disposable, 1-3/16" O.D., 2.625" L
FDA UDI
A-M SYSTEMS, LLC·00817081023756·Mouthpiece, Disposable, 1-3/16" O.D., 2.625" L
SurgiMac
FDA UDI
Surgimac LLC·D105SKU1626020·Goldman Fox TC, curved, Scissors, Pro Series.
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383561549·Gutta Percha Points is used to root canal filin...
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383539951·Gutta Percha Points is used to root canal filin...
SurgiMac
FDA UDI
Surgimac LLC·D105SKU1626030·Goldman Fox TC, straight, Scissors, Pro Series.
1ML BD SAFETY-LOK¿ U-100 INSULIN SYRINGE WITH 29 G X 1/2" BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·July 20, 2017
1ML BD SAFETY-LOK¿ U-100 INSULIN SYRINGE WITH 29G X 1/2" BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·February 2, 2017
BAND-AID(R) BRAND LIQUID BANDAGE
FDA 510(k)
FDA Class 1
·General Hospital
S6 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 24, 2025
8-CHANNEL ADAPTER, MDT, 10CM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·January 2, 2026
1ML BD SAFETY-LOK¿ U-100 INSULIN SYRINGE WITH 29 G X 1/2" BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·November 22, 2016
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·January 19, 2010
CONCERTO II CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·July 14, 2011
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JGS·June 11, 2013
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·January 19, 2010
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·January 19, 2010