23 results · 29ms · Sources: EU EUDAMED, US FDA

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BLOOD-SMEARING INSTRUMENT (MINIPREP TM)

FDA 510(k)
FDA Class 1 ·Hematology

Washbon

FDA UDI
ORMCO CORPORATION·00889989043044·LOWER LEFT SECOND MOLAR WASHBON BAND SIZE 7

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600071·Mand. 2. Bicuspidband left 07

RIBFIX BLU SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00841036197780·

RIBFIX BLU SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00888233011402·

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600070101·Mand. 2. Bicuspidband left 07

Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K0600070·Tray Insert, 1.5" Blank

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600070501·Mand. 2. Bicuspidband left 07

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR87600070051·Mand. 2. Bicuspidband left 07

BD AUTOSHIELD PEN NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Paclitaxel Sets

FDA 510(k)
FDA Class 2 ·General Hospital

CLEARLINK PACLITAXEL SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·February 2, 2024

CLEARLINK SOLUTION ADMINISTRATION SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 27, 2022

CLEARLINK SOLUTION ADMINISTRATION SETS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 27, 2022

RIBFIX BLU SYSTEM TEMPORARY FIXATION SCREW

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code HRS·August 3, 2018

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·April 18, 2014

21MM MOD REV HIP BDY/BLT +30MMCOMPONENT LEVEL 9006

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS CORK·Product code LZO·September 20, 2012

CE INFUSOR LV 5, 12 PACK

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·July 16, 2010

BD INSULIN PEN NEEDLE

FDA Adverse Event
Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories. This information may be used by a trained healthcare professional as a diagnostic tool for the visualization and analysis of anatomical and pathological structures.

FDA Enforcement
Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·March 29, 2017