26 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Econsole1
FDA 510(k)
FDA Class 2
·Radiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283785·
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690124146·Modular Offset Stem 11mm x 75mm x 2mm
Simpact Tri-Fin
FDA UDI
Life Spine, Inc.·00190837063085·Depth Gage
UniTip Catheter
FDA UDI
Unisensor AG·07640172973875·
ENDURANCE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295057352·FEMORAL STEM 12/14 TAPER ENDURANCE HIP STEM SIZ...
UniTip Catheter
FDA UDI
Unisensor AG·07640172973790·
HHF1 MAGNETIC RESONANCE IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MSA HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
WAVEWRITER ALPHA? PRIME 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 11, 2026
TRULIANT TIB IMP PSC INSERT SZ 6, 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 11, 2024
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
COLLEAGUE PRE 1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
URETEX TO2 URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·May 29, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code CAW·October 8, 2014
ProScreen 10 Panel Dip Card, Item No. PSD-10MOX, PSD-10MOB, PSD-10MMO300
FDA Enforcement
Class III
·Terminated·Ameditech Inc·December 30, 2015
TRULIANT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 24, 2024
ADVANCED PATELLA 29M 3 PEG IMPLANT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 15, 2024
TRULIANT TIB IMP PS INSERT SZ 2.5 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 14, 2023
ADVANCED PATELLA 32MM 3 PEG IMPLANT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 19, 2025