38 results · 31ms · Sources: EU EUDAMED, US FDA

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SYNTHES (USA) 1.3 MM CRANIOFACIAL SCREWS

FDA 510(k)
FDA Class 2 ·Dental

CD HORIZON® Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074034652·BONE SCREW 7021850 10 DEG ILC 8.5X50 SS

Safco FG Diamonds

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310218503·FG Diamond 885-012 beveled cylinder fine (gold)...

GPF-29 GENERAL PURPOSE COIL SET

FDA 510(k)
FDA Class 2 ·Radiology

RECORDING AND STIMULATING ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code LZG·January 15, 2019

28MM DIA COCR MOD HD +12MM NK

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·March 26, 2013

7700

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 25, 2011

LINOX S 75

FDA Adverse Event
Malfunction ·BIOTRONIK GMBH AND CO.·Product code LWS·March 28, 2008

GMK SPHERE CEMENTLESS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·May 25, 2026

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 21, 2024

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 5, 2025

GMK 3D METAL TIBIAL TRAY

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 6, 2025

GMK SPHERIKA CEMENTLESS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·December 19, 2025

GMK SPHERIKA CEMENTLESS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·December 24, 2025

GMK 3D METAL TIBIAL TRAY

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·January 23, 2026

GMK 3D METAL TIBIAL TRAY

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 11, 2025

GMK SPHERE TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 19, 2024

GMK SPHERIKA CEMENTLESS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MBH·January 24, 2025

SORIN BIOMEDICA SMARXT BCD VANGUARD

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTR·November 20, 2019