2,256 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260490·
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304462939·
Bernafon
FDA UDI
Bernafon AG·05711584086926·ZR3, KIT 312 NFM R BE ZERENA 3
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009621·2.0mm x 18mm Cannulated Lag Screw
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070249·Cannulated 2.0 x 18mm Lag Screw Sterile Qty 5
OMNIPRO INCLINE
FDA 510(k)
FDA Class 2
·Radiology
NORIAN REINFORCED, NORIAN REINFORCED FAST SET PUTTY
FDA 510(k)
FDA Class 2
·Neurology
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·April 11, 2018
640G INSULIN PUMP MMT-1711K
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·September 29, 2022
ARTICUL/EZE BALL 28 + 1.5 GR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDI·October 6, 2008
ZIMMER M/L TAPER FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LZO·June 20, 2013
SCULPTRA
FDA Adverse Event
AVENTIS PHARMA GRUPPO LEPETIT S.R.L.·Product code LMH·July 29, 2011
HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·February 22, 2018
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS LLC·Product code OYC·July 5, 2018
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code OYC·January 11, 2018
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·March 21, 2018
BA400 ABUTMENT 10MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 18, 2018
BIA400 IMPLANT 4MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·January 18, 2018