31 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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iASSIST Knee System
FDA 510(k)
FDA Class 2
·Neurology
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583032764·ET40, KIT 10 75 PB BE ENCHANT 40
Ceramco® II Silver™
FDA UDI
Dentsply International Inc.·D0011920800·
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788023629·20g TW x 8.0" Coudé® Blunt Nerve Block Needle w...
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 80mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665036510·
ID NOW COVID-19 2.0 Control Swab Kit
FDA UDI
Alere Scarborough, Inc.·00811877011361·Control Swabs intended for use only with the ID...
ORTHOFIX MODULSYSTEM
FDA UDI
ORTHOFIX SRL·18053340345194·SS TRANSFIXING PIN L260MM D4MM THREAD D5XL80MM QC
ORTHOFIX MODULSYSTEM
FDA UDI
ORTHOFIX SRL·18053340345217·SS TRANSFIXING PIN L260MM D4MM THREAD D5XL80MM ...
DEPUY RECLAIM REVISION HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PRESERVE HIP STEM
FDA 510(k)
FDA Class 3
·Orthopedic
BD PANEL PHOENIX NMIC-311
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 25, 2023
UNKNOWN DEPUY TIBIAL INSERT
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 27, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·October 7, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020