21 results · 36ms · Sources: EU EUDAMED, US FDA

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MULTI-DAY ELECTRODES

FDA 510(k)
FDA Class 2 ·Neurology

K2-HF OPAQUER powder, O-C1, 20g.

FDA UDI
Yeti Dentalprodukte GmbH·EYET38620110·

Shoreline™ ACS

FDA UDI
Seaspine Orthopedics Corporation·10889981177362·Modular Trial, 20 x 15 x 11mm, 7 Deg Lordosis

Symmetry Iris

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482128039·Symmetry® Scissors, Iris, Straight, Serrated, B...

MedDream

FDA 510(k)
FDA Class 2 ·Radiology

MODIFICATION TO FLOWSCREEN

FDA 510(k)
FDA Class 2 ·Anesthesiology

VerSys®

FDA UDI
Zimmer, Inc.·00889024173255·

VerSys®

FDA UDI
Zimmer, Inc.·00889024173248·

VerSys®

FDA UDI
Zimmer, Inc.·00889024138827·

VerSys®

FDA UDI
Zimmer, Inc.·00889024138810·

VerSys®

FDA UDI
Zimmer, Inc.·00889024366763·

VerSys®

FDA UDI
Zimmer, Inc.·00889024173262·

VerSys®

FDA UDI
Zimmer, Inc.·00889024138803·

VerSys®

FDA UDI
Zimmer, Inc.·00889024138797·

FEMORAL HEAD 12/14 TAPER

FDA Adverse Event
Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·March 17, 2020

SCREW,FIXATION,BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·May 18, 2015

SPECTTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 23, 2014

INTEGRATED APD SET W/CASSETTE3-PRONG

FDA Adverse Event
BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2010

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·October 31, 2012

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·July 27, 2015