24 results · 23ms · Sources: EU EUDAMED, US FDA

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BACT/ALERT FA PLUS CULTURE BOTTLE

FDA 510(k)
FDA Class 1 ·Microbiology

Spherodon - M

FDA UDI
SILMET LTD·07290012207273·Dental Amalgam Capsules

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450413418·

MaxFuse VBR, 10 (D) x 12 (W) x 63 (H)

FDA UDI
Pioneer Surgical Technology, Inc.·00846468055813·10 (D) x 12 (W) x 63 (H)

ATLANTIS VISION ANTERIOR CERVICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BD DIRECTIGEN EX FLU A+B

FDA 510(k)
FDA Class 2 ·Microbiology

LINEAR? ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 22, 2025

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929045176·Corpectomy, 12Dx14Wx61H 6°

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929064955·Corpectomy, 12Dx14Wx61H 0°

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·July 2, 2018

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWQ·June 13, 2018

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·July 29, 2014

LIGASURE ATLAS HANDSWITCHING 37CM

FDA Adverse Event
Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·May 6, 2011

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·March 31, 2018

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 28, 2018

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 2, 2014

XACT CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code NIM·June 16, 2023