16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OIC CANNULATED SCREW SYSTEM, OIC SLIDING HIP SCREW (SHS) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
JOBST forMen Casual
FDA UDI
BSN MEDICAL, INC.·00035664131234·FOR MEN CASUAL 20-30 MM HG KNEE HIGH CLOSED TOE...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613032623·Rasp, Down Cut, Straight, Concave, 15/16" x 1/4...
EMS PULMONARY FUNCTION TESTING FILTER
FDA 510(k)
FDA Class 2
·Anesthesiology
APEX POINTER+; MEASRUING CABLE, HOOK, LIP CLIP, TOUCH PROBE (ACCESSORIES)
FDA 510(k)
FDA Unclassified
·Unknown
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·January 11, 2001
PLUM A+ DRIVER REFUR
FDA Adverse Event
Malfunction
·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·May 9, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 20, 2011
EVITA DURA2
FDA Adverse Event
Malfunction
·DRAEGER MEDICAL AG & CO. KGAA·Product code CBK·August 1, 2008
UNKNOWN SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015
ACHIEVE MAPPING CATHETER - 20 MM
FDA Adverse Event
Injury
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code DRF·July 16, 2024
FLEXCATH ADVANCE STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRA·July 16, 2024
ONE TOUCH ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·July 27, 2009
EMBLEM S-ICD Model A209
FDA Enforcement
Class I
·Terminated·Boston Scientific Corporation·February 17, 2021
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021
Model Number L231, PROPONENT DR EL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025