26 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SONIXGPS
FDA 510(k)
FDA Class 2
·Anesthesiology
Z Liquid HT A1-C 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121812·Dental porcelain/ceramic restoration kit
NA
FDA UDI
Smith & Nephew, Inc.·03596010064776·4.0MM PARTIALLY THREADED CANNULATED SCREW 12MM
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675121812000·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311218120·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B1675121812070·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321218120·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167512181207A0·
TALOS®-C
FDA UDI
MEDITECH SPINE, LLC·B167512181200A0·
LEFORTE NEURO SYSTEM BONE PLATE
FDA 510(k)
FDA Class 2
·Neurology
CONSTRUX MINI PEEK SPACER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Chalgren
FDA UDI
CHALGREN ENTERPRISES·00816020020290·Ground/Reference Needle Electrode, EMG, 12mm x 28g
ACCELERATOR A3600
FDA Adverse Event
Malfunction
·INPECO SA·Product code JQP·December 20, 2024
Ascendant
FDA UDI
Choice Spine, LP·10885862261199·
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code DTK·May 21, 2013
SOFTHEAT
FDA Adverse Event
Malfunction
·KAZ USA, INC.·Product code IRT·July 28, 2014
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code CFR·May 20, 2011
NRG TRANSSEPTAL NEEDLE
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DXF·December 16, 2020
HEARTWARE VENTRICULAR ASSIST SYSTEM- PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·August 15, 2018
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF GROUP A STREP CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code GTY·March 31, 2025