28 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAVEX ORTHOTRACE
FDA 510(k)
FDA Class 2
·Dental
N/A
FDA UDI
GEORGE TIEMANN & CO.·B58212070·HOLDER, NEEDLE, GASTROENTEROLOGIC
PALACOS®
FDA UDI
Heraeus Medical GmbH·04260102135826·PALACOS® MV+G is indicated for use as bone ceme...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm
LASER PERIPHERALS REUSABLE HOLMIUM FIBER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STARLIGHT
FDA 510(k)
FDA Class 2
·Neurology
EVIS EXERA III BRONCHOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code EOQ·April 7, 2026
ATTAIN OTW
FDA Adverse Event
Injury
·MPRI·Product code LWP·April 10, 2013
ICEMAN THERAPY UNIT
FDA Adverse Event
Injury
·DJ ORTHOPEDICS DE MEXICO·Product code ILO·April 6, 2011
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·May 23, 2008
PERSONA ARTICULAR SURFACE MEDIAL CONGRUENT (MC)
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·September 30, 2024
PERSONA ALL-POLY PATELLA
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code MBH·September 30, 2024
PERSONA FEMUR CEMENTED CRUCIATE RETAINING (CR)
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code JWH·September 30, 2024
PERSONA CEMENTED TIBIA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 30, 2024
OPTETRAK HI-FLEX TIBIAL INSERT SZ 3 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 27, 2024
TIBIA CEMENTED 5 DEGREE STEMMED RIGHT SIZE C
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·June 3, 2025
ALL-POLY PATELLA CEMENTED 29 MM DIAMETER
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code MBH·June 3, 2025
FEMUR CEMENTED (CR) STANDARD NITRIDED RIGHT SIZE 7
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·June 3, 2025
ARTICULAR SURFACE (MC) RIGHT 10 MM HEIGHT
FDA Adverse Event
Injury
·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code MBH·June 3, 2025
ACTIVA
FDA Adverse Event
Malfunction
·MPRI·Product code MHY·June 28, 2021