48 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VARIAX ELBOW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
eTRAX™ Needle
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436101851·Sterile needle, 16GA x 17.7cm with (7.6 tapered...
Zavation
FDA UDI
Zavation LLC·00842166185203·Adjustable Drill Guide
OsteoMed
FDA UDI
OSTEOMED LLC·00845694033428·Lone Surgeon Plate 2.2mm, 0 Degree, Mini, 4 Hol...
KRATZ-BARRAQUER WIRE SPECULUM
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072152·KRATZ BARRAQUER WIRE SPECULUM SMALL SIZE OPEN W...
OLYMPIC WARM-UP
FDA 510(k)
FDA Class 2
·Physical Medicine
ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
FDA 510(k)
FDA Class 2
·Cardiovascular
VERCISE GEVIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code MHY·November 20, 2023
TAPERLC BMPC LAT 6.0X132 12/14
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·August 4, 2016
TAPERLOC PC 15.0 MM 12/14
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·August 4, 2016
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 9, 2013
GRANUFLO
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 24, 2011
ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025
TAPERLOC COMPLETE MICROPLASTY FEMORAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017
STOCKERT S3 GAS BLENDER
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014
TPRLC 133 TYPE1 BM SO 11.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018
TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·May 26, 2017
TAPERLOC TYPE1 BM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018
TPRLC 133 FP TYPE1 BM HO 10.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018