26 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HLS NOETOS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450649510·
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036011239·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033540961·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033540978·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033541159·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033540954·
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HXW·April 13, 2020
MODIFICATION TO FLUROTEX SURGICAL MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254
FDA 510(k)
FDA Class 2
·Cardiovascular
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HXW·April 13, 2020
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HXW·June 22, 2020
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HXW·October 22, 2019
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HXW·October 21, 2019
OPS FIBER 55CM SPOTLIGHT
FDA Adverse Event
Malfunction
·ANGIODYNAMICS·Product code GEX·July 28, 2022
PORTASCAN
FDA Adverse Event
Malfunction
·MEDIWATCH UK LTD·Product code ITX·November 17, 2011
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code MTA·March 20, 2013
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE HEALTHCARE SURGERY·Product code JAA·March 18, 2008
PECTUS TABLE TOP BENDER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·August 8, 2018