396 results · 33ms · Sources: EU EUDAMED, US FDA

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Hepatitis A Test (Antibody And Igm Antibody)

FDA Pre-Market Approval
FDA Class 2 ·ADVIA CENTAUR HAV TOTAL ASSAY, ADVIA CENTAUR HAV TOTAL QUALITY CONTROL MATERIALS

Leksell Vantage Stereotactic System

FDA UDI
Elekta Solutions AB·07340201501283·FirmFix™ 2

FirstPlug

FDA UDI
35newtons L.L.C.·00860005367207·FirstPlug Screw Channel Barrier 210 cm

23GA Illuminating Laser Probe, SMA906

FDA UDI
Peregrine Surgical, Llc·00632307001819·23GA Illuminating Laser Probe, SMA906

FirstPlug

FDA UDI
35newtons L.L.C.·00860005367221·FirstPlug Screw Channel Barrier 210 cm

FirstPlug

FDA UDI
35newtons L.L.C.·00860005367238·FirstPlug Screw Channel Barrier 210 cm

FirstPlug

FDA UDI
35newtons L.L.C.·00860005367252·FirstPlug Screw Channel Barrier 210cm

Multicare Platinum

FDA UDI
Hologic, Inc.·15420045505926·

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710820400170·Zadik Calcaneal Guide, 40mm x 17°

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710310400170·Talar Osteotmy Guide, 40mm x 17mm

ABC CAUDAL AND CRANIAL EXTENSION PLATE (E-PLATE)

FDA 510(k)
FDA Class 2 ·Orthopedic

INFINION CX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 14, 2023

ARTICULEZE M HEAD 36MM +5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·April 8, 2013

U BY KOTEX CLICK TAMPONS

FDA Adverse Event
Malfunction ·AVENT S. DE R.L. DE C.V.·Product code HEB·March 9, 2011

EASY LOAD INSERTION DEVICE

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code MSS·May 6, 2008

BD ONCLARITY HPV ASSAY REAGENT PACK

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024

BD ONCLARITY HPV ASSAY REAGENT PACK

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024

BD ONCLARITY HPV ASSAY REAGENT PACK

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MAQ·September 12, 2024

VERIFLEX¿

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·January 10, 2013

VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·June 17, 2010