11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MARCHETTI-VICENZI INTRAMEDULLARY NAIL, HUMERAL
FDA 510(k)
FDA Class 2
·Orthopedic
IMMUNODIFFUSION BAND INTENSIFYING FLUID
FDA 510(k)
FDA Class 2
·Microbiology
Tangible Hydrogel with Tangible Polymer (etafilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens
FDA 510(k)
FDA Class 2
·Ophthalmic
SS COMPRESSION HIP SCREW LAG SCREW
FDA Adverse Event
Injury
·BIOMET TRAUMA·Product code KTT·September 19, 2016
IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·June 14, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·March 2, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDB·February 9, 2017
PROSIMA PELVIC FLOOR REPAIR KIT
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·February 21, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 1, 2014
LIFEVEST WCD 3100 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·January 20, 2011