191 results · 20ms · Sources: EU EUDAMED, US FDA

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AMEDICA DRUG SCREEN METHAPHETAMINE TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

PERMITE

FDA UDI
SDI LIMITED·DO3640231012·

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668113776·AIR INJECT CANNULA 27GA

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00888233025164·

ALLOGENIX

FDA UDI
BIOMET MICROFIXATION, INC·00841036125844·

NA

FDA UDI
STERILMED, INC.·10888551017756·SAW BLADE INTRA ORAL COARSE

MICROCHOICE

FDA UDI
Conmed Corporation·10845854006627·MICROCHOICE OSCILLATOR INTRA-ORAL BLADE 11.5 X ...

MEDTEXX POWDERFREE NITRILE RUBBER EXAMINATION GLOVES, GREEN COLOUR

FDA 510(k)
FDA Class 1 ·General Hospital

WIENER LAB. AMILASA 405 CINETICA AA, WIENER LAB.AMILASA 405 CINETICA UNITEST,WIENER LAB.AMILASA CINETICA AA

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ORTHO SUMMIT SAMPLE HANDLING SYSTEM

FDA Adverse Event
Malfunction ·HAMILTON BONADUZ AG·Product code JTC·February 1, 2000

PLUM A+3 V11.51 REFR

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 26, 2013

LEAD NEURO

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·February 24, 2011

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE LTD·Product code FRN·April 3, 2008

WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·May 24, 2023

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

EVIS EXERA III DUODENOVIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·August 19, 2025