BEUDAMED
    28 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.
    Filters Regulation: Us FDA ×

    SURGIMESH XB - SKIRTED

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

    NeuroPEN

    FDA UDI
    CLARUS MEDICAL, LLC·00810004820678·NeuroPEN, Short, 15.5cm Working Length

    NeuroPEN

    FDA UDI
    MEDTRONIC PS MEDICAL, INC.·00613994840233·NEUROPEN 2120-025 15MM 15.5 DF .045

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057372193·Finger Trap Small

    RIVA Posterior Fixation System

    FDA UDI
    XENIX MEDICAL LLC·00840493418544·CONSTRAINED LORDOTIC ROD, 5.5mm x 25mm

    RIVA Pedicle Screw System

    FDA UDI
    XENIX MEDICAL LLC·00840493418759·CONSTRAINED LORDOTIC ROD, 6.0mm x 25mm

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707008873·CALIBRA 1ST MOLAR BANDS n.UR 25

    COMBAT READY CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECTRA MICRODOSE MAMMOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Radiology

    LUXTEC

    FDA Adverse Event
    Malfunction ·INTEGRA YORK PA INC.·Product code EQH·January 29, 2012

    Widex

    FDA UDI
    Widex A/S·05706069796704·Widex EVOKE E-CIC (Light beige ) 220, Right, RC...

    Widex

    FDA UDI
    Widex A/S·05706069886863·WIDEX MOMENT M-XP (Light beige ) 220, Telecoil

    Widex

    FDA UDI
    Widex A/S·05706069796933·Widex EVOKE E-XP (Light beige ) 220, Telecoil, ...

    Widex

    FDA UDI
    Widex A/S·05706069888737·WIDEX MOMENT M-CIC (Light beige ) 220, Right

    Widex

    FDA UDI
    Widex A/S·05706069797992·Widex D-CIC (Light beige ) Dream 220, Right, RC...

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·December 29, 2025

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 6, 2018

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 8, 2011

    MICROSTAAR INJECTOR

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code KYB·August 14, 2008