24 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

METAMORPHOSIS

FDA 510(k)
FDA Class 2 ·Dental

CoRoent

FDA UDI
Nuvasive, Inc.·00887517596994·CoRoent Large MP Ti, 10x9x23mm 8°

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450216149·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450217641·

7L5s Ultrasonic Transducer(FDA)

FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904089010·

Orthopedic Instruments

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258694719·

EVOLIS 3031.0003 CEMENTLESS TIBIAL BASEPLATE SIZE 3

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2023

D.SIGN 96

FDA 510(k)
FDA Class 2 ·Dental

FREEDOM, MODEL 4660

FDA 510(k)
FDA Unclassified ·Unknown

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2011

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 29, 2011

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·January 14, 2011

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·April 13, 2011

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·September 9, 2011

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 14, 2011

EVOLIS STD FEMUR TI PLASMA SPRAYED RIGHT SIZE 4

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2019

EVOLIS TIBIAL BASE PLATE TI PLASMA SPRAYED

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code JWH·February 21, 2014

S-ROM*SCREW,6.5MM DIA,20MM LG

FDA Adverse Event
Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code LPH·May 3, 2013

TRIATHLON PS X3 TIBIAL INSERT

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·May 12, 2011