23 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WEGO-PGLA RAPID
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Cavitron®
FDA UDI
Dentsply Professional·D00381830011·Cavitron® Steri-Mate® Detachable Sterilizable H...
ArthroCare
FDA UDI
Provision·B504AEA1830010·
Arthrocare
FDA UDI
Provision·00810041063106·
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1230010·Rod Holder, Straight, 5.5 mm
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197499453·Harken Valves, paired
50x47m...
NA
FDA UDI
STRYKER CORPORATION·04546540939876·2108 Series Sagittal Blade Flared, Ground (29....
SYSTEM, BALLOON, INTRA-AORTIC AND CONTROL
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·November 17, 2023
ROCKWOOD CLAVICLE PINS
FDA 510(k)
FDA Class 2
·Orthopedic
M5 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
TRIFUSE
FDA Adverse Event
Malfunction
·ICU MEDICAL·Product code FMG·October 3, 2017
9" SMALLBORE EXT SET W/CLAVE®, CLAMPS, ROTATING LUER
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·April 5, 2019
NITREX GUIDEWIRE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DQX·February 28, 2025
CARDIOSAVE HYBRID, TYPE G PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·December 8, 2025
LOW PRESSURE BLACK MAX HANDPIECE
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBB·October 17, 2014
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS·Product code LYJ·June 21, 2013
MITEK VAPR GENERATOR
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code GEI·July 28, 2011
9" SMALLBORE EXT SET W/CLAVE®, CLAMPS, ROTATING LUER
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·June 5, 2019
CARDIOSAVE HYBRID TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·April 30, 2021