BEUDAMED
    17 results · 28ms · 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 ×

    STERILE BASIN SETS

    FDA 510(k)

    Mini Twin

    FDA UDI
    Rmo, Inc.·00885797674111·MBT MINI LP 018 HK/345 5-5 20EA

    SleepmateVelstretch Band Kit, Pediatric

    FDA UDI
    Ambu A/S·05707480041503·Pediatric Velstretch Band Kit

    FG Dental Burs

    FDA UDI
    BIOLINE DENTAL IMPLANT SYSTEMS LTD·07290119311057·

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848130120·Self-Drilling Screw - Ø1.5 mm x 4 mm

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310813012CFG1·NTI Diamond Coarse FG

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7402813012·Rampart-O

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0130120·Segmental Rod Reducer Driver

    vascuCAP

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROMOS MODULAR SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAXCUT DIAMOND BURS (6/pk) CRS 6813-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D7781006813121·MAXCUT DIAMOND BURS (6/pk) Shape: Amalgam; Size...

    MAXCUT DIAMOND BURS (6/pk) MED 813-012

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D778100813121·MAXCUT DIAMOND BURS (6/pk) Shape: Amalgam; Size...

    PENUMBRA SYSTEM 5MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·May 15, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012

    ADJ PIN COLLET 2.0-3.2MM

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·August 11, 2010

    BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51 13013 ENDO MODULAR CERAMIC MD 38 13019 ENDO MODULAR CERAMIC MD 51 13007 ENDO MODULAR CERAMIC SH 41 13008 ENDO MODULAR CERAMIC SH 43 13009 ENDO MODULAR CERAMIC SH 45 13010 ENDO MODULAR CERAMIC SH 47 13011 ENDO MODULAR CERAMIC SH 49 13014 ENDO MODULAR CERAMIC MD 41 13015 ENDO MODULAR CERAMIC MD 43 13016 ENDO MODULAR CERAMIC MD 45 13017 ENDO MODULAR CERAMIC MD 47 13018 ENDO MODULAR CERAMIC MD 49 14823 ENDO MODULAR CERAMIC SH 53 14824 ENDO MODULAR CERAMIC MD 53 14825 ENDO MODULAR CERAMIC SH 55 14826 ENDO MODULAR CERAMIC MD 55 17295 ENDO MODULAR CERAMIC SH 36 17296 ENDO MODULAR CERAMIC MD 36

    FDA Recall
    Open, Classified ·BioPro, Inc.·Product code LZY·September 9, 2025

    BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51 13013 ENDO MODULAR CERAMIC MD 38 13019 ENDO MODULAR CERAMIC MD 51 13007 ENDO MODULAR CERAMIC SH 41 13008 ENDO MODULAR CERAMIC SH 43 13009 ENDO MODULAR CERAMIC SH 45 13010 ENDO MODULAR CERAMIC SH 47 13011 ENDO MODULAR CERAMIC SH 49 13014 ENDO MODULAR CERAMIC MD 41 13015 ENDO MODULAR CERAMIC MD 43 13016 ENDO MODULAR CERAMIC MD 45 13017 ENDO MODULAR CERAMIC MD 47 13018 ENDO MODULAR CERAMIC MD 49 14823 ENDO MODULAR CERAMIC SH 53 14824 ENDO MODULAR CERAMIC MD 53 14825 ENDO MODULAR CERAMIC SH 55 14826 ENDO MODULAR CERAMIC MD 55 17295 ENDO MODULAR CERAMIC SH 36 17296 ENDO MODULAR CERAMIC MD 36

    FDA Enforcement
    Class II ·Ongoing·BioPro, Inc.·October 22, 2025