16 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CMOS Video Rhino-Laryngoscope SSU
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583032405·ET40, KIT 312 2.4G NFM 90 R BE ENCHANT 40
Ceramco® II Silver™
FDA UDI
Dentsply International Inc.·D0011920900·
GALILEO® LEFTY TIGHTY™ CRT²™ LAG SCREW, LEFT, 10.5mm x 90mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665036534·
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780418979·Integra® Miltex® Micro Ear Forceps, Oval Cup Jaws
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780418986·Integra® Miltex® Micro Ear Forceps, Oval Cup Ja...
SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ERBELIFT HAND PUMP AND FLEXIBLE PROBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LEFTY TIGHT LAG SCREW, Ø10.5MM X 90MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·February 3, 2025
LEFTY TIGHT LAG SCREW, Ø10.5MM X 90MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·August 10, 2022
LEFTY TIGHT LAG SCREW, Ø10.5MM X 90MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HSB·August 18, 2022
LEFTY TIGHT LAG SCREW, Ø10.5MM X 90MM
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code HSB·August 21, 2024
LIFESHIELD NV PRIMARY PIGGYBACK SET
FDA Adverse Event
Injury
·HOSPIRA LTD.·Product code FPA·October 7, 2008
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013
RF3000 RADIOFREQUENCY GENERATOR
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·August 4, 2011
COMP PRIMARY STEM 4MM MINI
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·October 15, 2020