32 results · 26ms · 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.

Fetal Doppler

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

Sonic

FDA UDI
Sonic Innovations, Inc.·05711583030029·ENCHANT 80 FW 1.0

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197032247·Potts-Smith Vascular Scissors 40° an...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197039765·Super-Cut Potts-Smith Vascular Scissors 45 ° a...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197176194·Antrum Curette oval small 2mm, 2...

WINSTIM

FDA 510(k)
FDA Class 2 ·Physical Medicine

BAXOLVE XP CONDUCTIVE GARMENT ACCESSORY & LUMBAR SUPPORT KIT, MODELS 297, 298

FDA 510(k)
FDA Class 2 ·Neurology

BV Medical

FDA UDI
BV Medical·00845821025838·EMT 5, Infant, Child, Adult, Large Adult, Thigh...

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 14, 2025

1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT

FDA Adverse Event
Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024

COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY WITH LOCKING RING

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 17, 2017

IDENTITY XL DR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 14, 2013

BMT 360 2.5MM OFFSET ADAPTER

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·November 8, 2018

OSSEOTITE XP IMPLANT 4/5 X 13MM

FDA Adverse Event
Injury ·BIOMET 3I·Product code DZE·November 27, 2024

ENDOSCOPIC LNR CUTR (EXACT CODE UNKNOWN)

FDA Adverse Event
Death ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 5, 2021

UNKNOWN KNEE TIBIAL INSERT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·August 8, 2023

PFC SIGMA CVD INSRT SZ2.5 10MM

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HAW·August 2, 2023