18 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSSIOfiber® Suture Anchor 2.5-3.5 mm
FDA 510(k)
FDA Class 2
·Orthopedic
Cascadia™ Interbody System
FDA UDI
VB Spine LLC·10888857369993·Trial, Size 12x14x9 mm, 30°
Tokuyama Universal Bond II
FDA 510(k)
FDA Class 2
·Dental
ABMD Software
FDA 510(k)
FDA Class 2
·Radiology
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 2, 2023
HARMONIC ACE + 7
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 11, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 29, 2011
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 23, 2013
BI-METRIC POROUS FMRL 14X150MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·May 1, 2019
M2A-MAGNUM MOD HD SZ 50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·May 1, 2019
M2A-MAGNUM RECAP CUP 56ODX50ID
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·May 1, 2019
RATTLER XL CANNULATED INTERFERENCE SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWC·January 9, 2018
RATTLER CANNULATED INERFERENCE SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HWC·January 9, 2018
ACT ARTIC E1 HIP BRG 28X48MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 22, 2019
M2A-MAGNUM PF CUP 54ODX48ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·August 22, 2019
MLRY-HD POR FMRL 10X155MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 22, 2019
UNK CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 29, 2019
UNKNOWN BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·January 29, 2019