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

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DR180-II

FDA 510(k)
FDA Class 2 ·Cardiovascular

Custom Procedure Kit

FDA UDI
MEDIVATORS INC.·40677964011502·Endo Carry-On Procedure Kit

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040044308·Knife Goldman Fox DE #11

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001288·artVeneer life lower anteriors, UBL, B4

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00012881·

Vista

FDA UDI
Modus Medical Devices Inc·G34350012881·40 mm PET jar with lid - box of 100

ULTRASIM CT SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

REICHERT CT200 CONTACT TONOMETER

FDA 510(k)
FDA Class 2 ·Ophthalmic

EVOLUTION MP CS INSERT SIZE 7 STANDARD 10MM LEFT

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·March 16, 2020

EVOLUTION MP CS INSERT SIZE 8 STANDARD 12MM LEFT

FDA Adverse Event
Malfunction ·MICROPORT ORTHOPEDICS INC.·Product code HRY·April 13, 2020

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·May 23, 2026

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·February 22, 2026

UNIVERSAL SLING BAR

FDA Adverse Event
Other ·LIKO AB·Product code FSA·February 28, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 24, 2011

LIFEVEST WCD 3000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 19, 2008

SYRINGE 20ML LL 120/PKG

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 4, 2020

ADVANCE® ONLAY ALL-POLY PATELLA 32MM TRI-PEG

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 1, 2022

EVOLUTION® NITRX? TIB KEELED

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022

EVOLUTION® NITRX? TIB KEELED

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·November 7, 2022

EVOLUTION® NITRX? FEM CS/CR NONPOR TINBN COATED SI

FDA Adverse Event
Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·December 14, 2022