22 results · 26ms · Sources: EU EUDAMED, US FDA

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SomnoDent Avant

FDA 510(k)
FDA Class 2 ·Dental

Vanguard Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304680579·

Vanguard Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304647817·

PRECISE SHP DIODE LASER

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

21.3 INCH (54 CM) MONOCHROME LCD MONITOR MS23I2 (ML21023)

FDA 510(k)
FDA Class 2 ·Radiology

TRUWAVE

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·April 22, 2026

VANGUARD CR FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

VANGUARD CR ILOK FEM-RT 65

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

BIOMET CC I-BEAM TRAY 71MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

UNKNOWN BIOMET ARCOM 3 PEG/POST SIZE 31

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

ARCHITECT C8000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·October 3, 2008

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·July 28, 2011

TRUWAVE

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES DR·Product code DXO·March 27, 2025

VANGUARD UNKNOWN KNEE PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

BIOMET CC I-BEAM TRAY

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

TRUWAVE

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·April 10, 2025

VANGUARD CR ILOK FEM-LT 65

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2019

SERIES A PAT STD 31 3 PEG

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2019

TRUWAVE

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·September 5, 2025