22 results · 26ms · Sources: EU EUDAMED, US FDA

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OLYMPUS RF LATEX CALIBRATOR, AND OLYMPUS RF LATEX REAGENT WITH MODEL(S): ODC0028, AND OSR61105.

FDA 510(k)
FDA Class 2 ·Immunology

“Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)

FDA UDI
Paonan Biotech Co.,Ltd.·04719878786881·Awl with Depth Stop

Mini-Mono®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70602011·Mini-Mono-Brackets Roth 'N' .022" 100 Brackets

MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0600010·Tray Insert, Level 1

Ocata Anterior Cervical System

FDA UDI
Kalitec Direct LLC·B07308K0600010·Tray Insert 1, Ocata

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·January 31, 2007

Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K0602000·Tray base, 2"

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·February 16, 2007

BAYER ADVIA IMS SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

HARDYDISK, STREPTOMYCIN 10MCG

FDA 510(k)
FDA Class 2 ·Microbiology

LAP DISC HAND ACCESS DEVICE

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·August 21, 2006

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code GIS·January 9, 2007

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·January 26, 2007

HOURGLASS

FDA Adverse Event
Injury ·MEDTRONIC·Product code MQP·June 16, 2014

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·October 20, 2006

PINN.SECTOR ACET.CUP 52MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS·Product code KWA·April 16, 2013

ENDURANT II EXTENSION CUFF

FDA Adverse Event
Injury ·MEDTRONIC IREALAND·Product code MIH·September 4, 2014

STARCLOSE SE VASCULAR CLOSURE SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·April 15, 2011

ALTO

FDA Adverse Event
Injury ·ELA MEDICAL, S.A.S.·Product code MRM·February 1, 2006

CONFIDA BRECKER CURVE GUIDEWIRE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DQX·June 5, 2025