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IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code LWS·August 12, 2023

CS300 INTRA-AORTIC PUMP

FDA Adverse Event
Injury ·DATASCOPE CORP.·Product code DSP·March 28, 2014

HYDROCOIL 10-SYSTEM COIL (HES)

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code HCG·March 27, 2009

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·July 8, 2025

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·December 3, 2024

UNKNOWN VICRYL RAPIDE SUTURE

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·December 3, 2024

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·June 2, 2025

Howmedica Osteonics Corp., Scorpio NRG Femoral Size 7 Right; Knee prosthesis (Stryker France). Product Code: 814407R. Mahwah, NJ

FDA Recall
Terminated ·Stryker Howmedica Osteonics Corp.·Product code JWH·August 20, 2007

GYNECARE MESH UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTM·January 23, 2026

CARDIOSAVE HYBRID

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 7, 2023

i-STAT PT/INR Cartridge Abbott Point of Care, Princeton, NJ

FDA Recall
Terminated ·Abbott Point of Care Inc.·Product code GJS·May 5, 2010

BD Vacutainer Urine Complete Kit with UA Preservative Tube and C&S Preservative Tube for Midstream Specimens PLUS Plastic, Sterile Cup and Tube Interiors. Store at 4-25 degrees C. For In Vitro Diagnostic Use. Becton Dickinson and Company, Franklin Lakes, NJ.

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JSM·October 12, 2009

BD Vacutainer Urine Complete Kit with UA Tube and S&C Preservative Tube for Midstream specimens; Plus Plastic - Sterile Cup and Tube interiors. Store at 4-25 degrees C. Kit contains Sterile Screw CAP Collection Cup with integrated Transfer Device and 8.0 mL, 16/x100 mm PLUS Plastic Conical Tube for Urinalysis and 4.0 mL 13x75mm Plus Plastic C&C Preservative tube and Castile Soap Towelettes; Becton Dickinson and Company, Franklin Lakes, NJ

FDA Recall
Terminated ·Becton Dickinson & Company·Product code JSM·October 12, 2009

Accessory, System, External Fixator, Containing Antimicrobial Agent

FDA classification
FDA Class 2 ·Accessory, System, External Fixator, Containing Antimicrobial Agent

NEA INTERNATIONAL BV

FDA registration
NEA INTERNATIONAL BV·5 products·🇳🇱 Netherlands

NOA MEDICAL INDUSTRIES

FDA registration
NOA MEDICAL INDUSTRIES·4 products·🇺🇸 United States

NJR MEDICAL, INC.

FDA registration
NJR MEDICAL, INC.·1 product·🇺🇸 United States

n.a.

FDA UDI
VBM Medizintechnik GmbH·04250105628760·Acceesory KIT for Manual Suction Pump

PIEZOsoft

FDA UDI
KaVo Dental GmbH·EKAV100984880·This is a medical device.

Prophylaxe Set 2008

FDA UDI
KaVo Dental GmbH·EKAV100703380·This is a medical device.