6,550 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Epsilon USA
FDA UDI
EPSILON EYE CARE PRIVATE LIMITED·G346EMF14P0·Micro Handle Colibri 0.12mm 1x2 Teeth Forceps W...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613082871·Micro Handle Colibri Forceps, Titanium, 0.12mm,...
Epsilon USA
FDA UDI
EPSILON EYE CARE PRIVATE LIMITED·G346EMF140·Micro Handle Colibri 0.12mm 1x2 Teeth Forceps (...
ORTHO DEVELOPMENT ORION-I EMF SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ENDOSCOPIC MONOPOLAR FORCEPS-SCISSORS, EMF-2000 TO 2999,ENDOSCOPICS MONOPOLARFOEPS-GRASPERS, EMF-3000 TO 3999, ENDOSCOPO
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NEUROSTIMULATOR IMPLANT
FDA Adverse Event
Malfunction
·UNK·Product code LGW·February 9, 2022
SPINE STIMULATIOR
FDA Adverse Event
Injury
·UNK·Product code LGW·April 9, 2026
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MRU·December 28, 2017
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·May 29, 2018
EMF PAL II MAIN GENERATOR AND IRRIGATION UNITS AND ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MRI
FDA Adverse Event
Injury
·PICKER INTL·Product code LNH·April 12, 1994
MEDTRONIC
FDA Adverse Event
Malfunction
·Product code LGW·July 18, 2011
MRI
FDA Adverse Event
Injury
·GE HEALTHCARE MANUFACTURING LLC·Product code LNH·March 23, 2026
STRYKER TRIDENT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS/HOWMEDICA OSTEONICS CORP·Product code LPH·September 8, 2025
PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
FDA Adverse Event
Injury
·STRYKER ORTHOPEDICS/HOWMEDICA OSTEONICS CORP·Product code LPH·September 8, 2025
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 14, 2022
PACEMAKER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWP·July 29, 2021
STRYKER SPINE XIA 4.5 TITANIUM ROD
FDA Adverse Event
Injury
·STRYKER SPINE·Product code JDN·May 28, 2008
QUANTUM
FDA Adverse Event
Malfunction
·INTERMEDICS, INC.·Product code DXY·September 15, 1994
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 21, 2008