BEUDAMED
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    BioZorb LP Marker

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

    Epredia

    FDA UDI
    RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063777·The blades and knifes consumables are for use w...

    LACTOSORB* 2.0MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036054250·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100189·MCINTYRE SPECULUM CLOSED WIRE

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111253027·OP SCISS CVD BL/BL 7"

    Trial Liners (Neutral and 10 degree hooded)

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215038663·

    CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.014 GUIDE WIRE, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.18 G

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATLANTIS ABUTMENT IN ZIRCONIA, ATLANTIS GEMINI ABUTMENT IN ZIRCONIA, ATLANTIS GEMEINI + ABUTMENT IN ZIRCONIA

    FDA 510(k)
    FDA Class 2 ·Dental

    Herbert/Whipple®

    FDA UDI
    Zimmer, Inc.·00889024033993·

    WAVEWRITER ALPHA? PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 5, 2025

    TRULIANT TIB IMP PSC INSERT SZ 6, 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 11, 2024

    FREESTYLE AORTIC ROOT BIOPROSTHESIS

    FDA Adverse Event
    Death ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·October 8, 2014

    UV FLASH TRANSFER SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 7, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·June 7, 2013

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

    METACROSS OTW PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

    OHICHO NEO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·December 26, 2019

    DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015