BEUDAMED
    86 results · 21ms · Sources: EU EUDAMED, US FDA

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    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen PDGFRA RGQ PCR Kit

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989044072·CROWN-PERM UL 2 MOLAR SST PK/5

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124358·LOCATOR R-Tx Attachment System for 3.5 Internal...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180175372·DOYEN RETRACTOR, BLADE SIZE 75MM X 35MM, SLIGHT...

    EdgePro

    FDA UDI
    Biolase, Inc.·00647529004135·An all-tissue dental laser system intended for ...

    EdgePRO™

    FDA UDI
    US ENDODONTICS, LLC·00818365026630·EdgePRO™ System 0

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301341·Silicone Handle, Egg, Medium 1/4" QC Modular, I...

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301426·Silicone Handle, Ball, Large 1/4" QC Modular, I...

    Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 218504 L210004 210005 218505 L210005 210006 218506 L210006 210007 218507 L210007 210015 218516 L210008 210016 218518 L210009 210017 218519 L210010 210018 218520 L210011 210019 218521 L210012 210020 218523 L210013 210023 218524 L210014 210024 218525 L210015 210025 218526 L210016 210026 218527 L210017 210027 218528 L210018 210028 218529 210029 210030

    FDA Recall
    Terminated ·C. R.Bard, Inc./Electrophysiology Division·January 8, 2003

    Universal Dilator

    FDA UDI
    SPINEOLOGY INC.·M7405210002·Pedicle Markers

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540225949·BONE SCREWS, CROSS-FIT, SELF-TAPPING

    STELLA BIO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD PHASEAL¿ INJECTOR LUER LOCK N35

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 15, 2023

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172139·Tribrid Femoral Instruments Case Tray

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523171989·Tribrid Femoral Instruments Case Base

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523171996·Tribrid Pin Caddy

    Tissue Adhesive For The Topical Approximation Of Skin

    FDA Pre-Market Approval
    FDA Class 2 ·INDERMIL(TM) TISSUE ADHESIVE

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)

    PERSONA®

    FDA UDI
    Zimmer, Inc.·00889024641877·

    PERSONA™

    FDA UDI
    Zimmer, Inc.·00889024239548·