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

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Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration System - Penumbra Engine Pump Canister

FDA 510(k)
FDA Class 2 ·Cardiovascular

Maestro™ Total Wrist

FDA UDI
Biomet Orthopedics, LLC·00887868239434·

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780165248·Integra® Jarit® Taylor Percussion Hammer, 7-3/4...

MAESTRO TOTAL WRIST

FDA UDI
Biomet Orthopedics, LLC·00880304439153·

LOCATOR R-Tx

FDA UDI
Zest Anchors, LLC·00840481122620·LOCATOR R-Tx Attachment System for 2.5mm Platfo...

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481122453·LOCATOR F-Tx Abutment for 2.5mm Platform Conica...

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889987169187·CORTICAL SHANK, Cannulated, 8.0 X 105

Mariner Cortical

FDA UDI
Seaspine Orthopedics Corporation·10889981169183·CORTICAL SHANK, Cannulated, 8.0 X 105

Super Upper Limbs Versalock Plating System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258665641·VERSALOCK TOTAL WRIST FUSION PLATE - DORSAL

Sochi

FDA UDI
Altus Spine, LLC·00843210173917·Rod, 3.5mm x 105mm

ENDOTRACHEAL TUBE

FDA 510(k)
FDA Class 2 ·Anesthesiology

BD PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Orthopedic Instruments

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258694535·

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·January 31, 2018

KINETRA

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·October 25, 2010

BD MICROLANCE¿ 3 NEEDLES

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·November 11, 2019

EVIS EXERA III COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·July 11, 2025

INSTINCT ENDOSCOPIC HEMOCLIP

FDA Adverse Event
Malfunction ·WILSON-COOK MEDICAL INC.·Product code MND·June 13, 2013

ONYX, AVM

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·July 27, 2011

ENDO GIA UNIVERSAL 12MM SINGLE USE INST

FDA Adverse Event
Injury ·NORTH HAVEN - USS·Product code GDW·September 29, 2008