BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ACETASITE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SCOTT'S SELECT TEMPORARY C&B STD PKG B1

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819312570·

    Pangea Utility Plating System, Pangea Platform

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SJM MASTERS SERIES MECHANICAL HEART VALVE

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL·Product code LWQ·June 20, 2014

    ASPHERE M SPEC 11/13 44 +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 28, 2013

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·December 17, 2010

    Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025