26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TAV Medical Dental Implants System
FDA 510(k)
FDA Class 2
·Dental
EarQ
FDA UDI
Oticon A/S·05707131318589·G50, MRITE 312 2.4G NFM PB C093 EARQ
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306820663·Castroviejo Scissors, Curved, Blunt/Blunt, 8mm ...
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131101·IN-OVATION® C Base Rx 018 U3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131611·IN-OVATION® C Roncone 018 U3-3 CS HK
RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS
FDA 510(k)
FDA Class 2
·Radiology
LAVA ULTIMATE CAD/CAM RESTORATIVE FOR CEREC / E4D, LAVA ULTIMATE IMPLANT CROWN RESTORATIVE
FDA 510(k)
FDA Class 2
·Dental
LINER: MPACT FLAT PE HC LINER Ø36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·July 9, 2019
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 4, 2017
CAPIOX FX OXYGENATOR
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 4, 2017
LINER: MPACT FLAT PE HC LINER Ø36/F
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·February 9, 2018
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 14, 2014
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORP·Product code LZG·June 6, 2013
UNK KNEE
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code JWH·June 22, 2011
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·February 4, 2020
DREAMSTATION AUTO CPAP
FDA Adverse Event
Injury
·RESPIRONICS INC·Product code BZD·May 5, 2022
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·January 2, 2020
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·February 4, 2020
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Injury
·COOK INC·Product code KRA·January 2, 2020
EXPRESSEW III AC+ GUN
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code LXH·January 5, 2022