23 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X
FDA 510(k)
FDA Class 2
·Orthopedic
Channels
FDA UDI
HENRY SCHEIN, INC.·10304040039059·Channels K-Files 21mm, #70
Affiniti™ EH²
FDA UDI
TORNIER, INC.·00846832002252·
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65820200851·Channels K-Files 21mm
AOS CANCELLOUS SCREW 6.5mm x 85mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665008043·
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306800092·Graduated Medicine Cup , 2 oz
A8 INTEGR8® Porous Pedicle Screw System
FDA UDI
ALLUMIN8, INC.·00850080774052·Tap: 8.5 mm
NA
FDA UDI
STRYKER CORPORATION·04546540755865·GRAFT SIZING GAUGE 6MM
ULTRASOUND SCANNER, TYPE 1101
FDA 510(k)
FDA Class 2
·Radiology
PORTSETT
FDA 510(k)
FDA Class 2
·General Hospital
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·April 1, 2025
TALENT THORACIC STENT GRAFT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·March 25, 2013
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·March 10, 2011
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC.·Product code LFR·May 25, 2007
UNKNOWN_NEUROVASCULAR_PRODUCT
FDA Adverse Event
Injury
·CONCENTRIC MEDICAL·Product code NRY·December 14, 2012
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·August 11, 2025
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·March 20, 2025
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·October 2, 2025
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·April 10, 2025
1.85MM TI MATRIX SCREW SELF-TAPPING/4MM
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code JEY·January 21, 2015