99 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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NON-CONTACT INFRARED THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780378297·Integra® Jarit® Adson Forceps, 4-3/4", Extra De...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450242421·
N/A
FDA UDI
Tyber Medical, LLC·M695M1302310·
DM
FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384335830·5 pieces
DM
FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384335837·5 pieces
CORONARY ARTERY PERFUSION CANNULA WITH SELF-INFLATING BALLOON
FDA 510(k)
FDA Class 2
·Cardiovascular
KYPHON INFLATION SYRINGE
FDA 510(k)
FDA Class 2
·Orthopedic
Widex
FDA UDI
Widex A/S·05706069908121·WIDEX MOMENT MRB2D DEMO (Silver Grey ) 330, Tel...
KP
FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384337070·6 pieces
KP
FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384337077·6 pieces
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 19, 2025
AEQ REV II GLENOID BASEPLATE DIA 25MM LONG POST
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code PHX·January 5, 2026
AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 18, 2023
AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 20, 2023
UNIVERSAL AO REAMER ATTACHMENT 250 RPM
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL S.A.·Product code HTO·May 22, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·September 30, 2014
KAPPA 700 DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011
AEQ REV II GLENOID BASEPLATE DIA 25MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·December 22, 2023
AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 14, 2026