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

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Custodiol HTK Solution

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

CoRoent

FDA UDI
Nuvasive, Inc.·00887517576439·CoRoent Ant TLIF Ti, 9x12x40mm 8°

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260698·

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304463271·

Orthos

FDA UDI
ORMCO CORPORATION·00889989030327·ORTHOS CM TMA 016 X 022 UPLG PK10

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009669·2.4mm x 8mm Cannulated Lag Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070546·Cannulated 2.4 x 8mm Lag Screw Sterile Qty 5

RHYTHM OF LIFE, MODEL R0901-05

FDA 510(k)
FDA Class 2 ·Cardiovascular

DIGITAL DIAGNOSTIC X-RAY SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MIDWEST LOW SPEED ATTACHMENTS - CONTRA ANGLE SHEATH

FDA Adverse Event
Malfunction ·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 20, 2023

OPTIPAC 60 REFOB BONE CMT R-3

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 11, 2026

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2013

BHR

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·August 5, 2011

ESSURE

FDA Adverse Event
Other ·CONCEPTUS, INC.·Product code HHS·September 30, 2008

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 22, 2025

REFOBACIN BONE CEMENT R 1X40-3

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 18, 2025

OPTIPAC 80 BIOMET BC R

FDA Adverse Event
Death ·BIOMET FRANCE S.A.R.L.·Product code LOD·April 9, 2026

BIOMET BONE CEMENT R 40 -3

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·July 31, 2025

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 17, 2025

OPTIPAC 60 REFOB BONE CMT R-3

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025