72 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SpiroScout
FDA 510(k)
FDA Class 2
·Anesthesiology
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486019990·MCK PF TEMPLATE (6 RIGHT)
OsteoMed
FDA UDI
Provision·00810041639462·
Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989029642·ARCH REV.CURVE NITI UP16 DIA. PK10
OsteoMed
FDA UDI
OSTEOMED LLC·00845694047739·Logic Distractor Left 18mm
OsteoMed
FDA UDI
Provision·B504OM31601160·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694032148·1.7mm Cannulated Drill, Long, Manual
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973106388·TRIAL 90-SRK-160116 POLY CR 1X16MM
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575390595·Surgical screwdriver, reusable - General instru...
Megasystem-C Tumor- and Revision System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575391608·Surgical screwdriver, reusable - Megasystem-C T...
CALIBRATED GUIDE WIRE, TROCAR POINT
FDA UDI
Biomet Orthopedics, LLC·00887868016165·
B-P TOTAL HIP SYSTEM
FDA UDI
ENDOTEC, INC.·00814193023872·B-P MODULAR EXTENSION W/ULTRACOAT - 16 MM X 25 MM
MICRUS COURIER MICROCATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
LASERTOUCHONE (OTC)
FDA 510(k)
FDA Class 2
·Neurology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694067980·Cannulated 1.7mm Drill, Long, Manual Sterile Qty 2
Widex
FDA UDI
Widex A/S·05706069923759·WIDEX MOMENT MBB3D 50 (Dark cherry)
INFINION 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 23, 2022
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024
EDWARDS SAPIEN TRANSCATHETER HEART VALVE
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code NPT·June 10, 2013
LINEAGE(R) DURAMER(R) ACETABULAR LINER
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·July 13, 2011