28 results · 20ms · Sources: EU EUDAMED, US FDA

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GIBRALT SPINE SYSTEMS FACET SCREW 04.0,04.5

FDA 510(k)
FDA Unclassified ·Unknown

N/A

FDA UDI
MEDTRONIC XOMED, INC.·00763000043162·PROSTHESIS 1112097 CAM CAP PARTL CANN

BioCare Safety Needles

FDA UDI
BIOTRONIX HEALTHCARE INDUSTRIES, INC.·00858835007776·Disposable BioGuard Safety Needles 23G x 1 1/2"

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756609999·Arm Sling

NA

FDA UDI
MEDTRONIC XOMED, INC.·00681490033411·PROSTHESIS 1112097 CAM CAP PARTL CANN

VORTEX

FDA 510(k)
FDA Class 2 ·Radiology

POWDER FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 17, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 21, 2025

CASPIAN Spinal System

FDA UDI
VB Spine LLC·10888857242395·Occipital Plate Bender (Short)

CASPIAN Spinal System

FDA UDI
VB Spine LLC·10888857242388·Occipital Plate Bender (Long)

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·June 2, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·March 27, 2025

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 31, 2012

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 10, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 17, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·August 6, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·March 25, 2025

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 31, 2012

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014