15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FUJIFILM Endoscope Model EB-710XT
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776181772·BRUNS CURETTE STR OVAL SIZE
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780187134·Integra® Jarit® Bruns Oval Cup Curette, 8", Str...
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925031883·DURAVENT VENTILATION TUBE TAPERED LUMEN WITH SP...
NA
FDA UDI
SYNTHES (U.S.A.) LP·10886982164841·SCALLOPED DISTAL TIBIA PLATE 15 HOLES
U2 FEMORAL COMPONENT, CR, POROUS COATED
FDA 510(k)
FDA Class 2
·Orthopedic
3DMetal Diaphyseal Femoral Cones
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 28, 2025
Widex
FDA UDI
Widex A/S·05706069827705·WIDEX EVOKE EBB3D (Lime green ) 440, Telecoil, ...
Widex
FDA UDI
Widex A/S·05706069692013·Widex BEYOND B-F2 (Lime green ) 440, Telecoil, ...
Duravent Silicone Ventilation Tube. Model Number: 240075.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·December 25, 2024
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 24, 2008
TENDRIL STS
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·September 9, 2011
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·July 11, 2013
Duravent Silicone Ventilation Tube. Model Number: 240075.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code ETD·November 19, 2024