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

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SecurePortIV Catheter Securement Adhesive

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

RESTORIS

FDA UDI
MAKO SURGICAL CORP.·00848486003500·MCK FEMORAL TRIAL (SIZE 5 LM/RL)

n.a.

FDA UDI
Karl Storz GmbH & Co. KG·04048551058282·TRAUTMANN Mastoid Gouge, 14 cm

LOCATOR F-Tx

FDA UDI
Zest Anchors, LLC·00840481122057·LOCATOR F-Tx Abutment For 6.0mm Platform Extern...

LEONE SPA

FDA UDI
LEONE SPA·08033707018674·CALIBRA 1ST MOLAR BANDS n.LL 5

KRYSTAL-X WIFI

FDA 510(k)
FDA Class 2 ·Dental

FRESENIUS 2008T HEMODIALYSIS MACHINE

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

LIGAMAX-5MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 21, 2011

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FPA·June 14, 2013

EVERA XT VR

FDA Adverse Event
Death ·MEDTRONIC INC.·Product code DTE·September 23, 2014

T-HANDLE INSERTER

FDA Adverse Event
Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·April 29, 2021

T-HANDLE

FDA Adverse Event
Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code LXH·May 2, 2023

IMPLANT INSERTER SH CONNECTION

FDA Adverse Event
Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·May 2, 2023

XL BLEU

FDA Adverse Event
Injury ·LEONHARD LANG GMBH·Product code DRX·September 20, 2017

CART 9734056 S7 STAFF SHRT 100-120V INTL

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·March 9, 2020

AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version: 24-10VA-1 Vivonic Part Number: G02000970-US

FDA Enforcement
Class II ·Ongoing·Fresenius Medical Care Holdings, Inc.·August 3, 2022