23 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRYKER UROLOGY AND GYNECOLOGY HARDWARE SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319718230·Spatula & Packer 5-1/2" (14cm), oval flat spatu...
Myo/Wire II
FDA UDI
A & E MEDICAL CORPORATION·10841291101987·SS Suture, 1 per sleeve
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981175610·Z-Rod, Dia. 5.5mm, Co-Cr, 390mm
VITAL SHIELD GOLD POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS
FDA 510(k)
FDA Class 2
·Cardiovascular
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·November 15, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 26, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 14, 2020
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·April 30, 2018
ETAC SWIFT MOBIL
FDA Adverse Event
Malfunction
·ETAC SUPPLY CENTER AB·Product code INM·March 12, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 15, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·May 7, 2008
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·May 8, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·February 2, 2021
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012