BEUDAMED
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    MODIFICATION TO INTRALASE 600C LASER KERATOME

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

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    INTACS CORNEAL IMPLANTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001211·artVeneer life upper anteriors, IXL, B2

    SCANLAN® Endoscopic TIP-GUARD™ instrument protectors - Clear

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159001952·SCANLAN® Endoscopic TIP-GUARD™ instrument prote...

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707126698·TRUFLEX NiTi Thermal Euro Lower 19x25 (10pk)

    Alpine

    FDA UDI
    Ortho Development Corporation·00822409000401·Alpine Cemented Stem 11 EXT

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730014009·NiTi Thermal Euro Lower 19x25 10 archwires per ...

    Health-Tec/DHP Hand Instruments

    FDA UDI
    Dental Health Products Inc·D77370012110·Health-Tec/DHP Elevator Heidbrink 2

    Silicone Tubing

    FDA UDI
    INVOTEC INTERNATIONAL, INC.·00818501023042·Silicone Tubing 0.125" X 0.250"

    QUICK-SET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 6, 2025

    PANORET, MODEL 1000A

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BUILD-IT FR

    FDA 510(k)
    FDA Class 2 ·Dental

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·February 24, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·July 8, 2014

    SYRINGE S2 2ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 23, 2020

    Colonoscope: for endoscopy and endoscopic surgery within the lower digestive tract (including the anus, rectum, sigmoid colon, colon and ileocecal valve). Model Numbers: CF-2T160I, CF-2T160L, CF-H170I, CF-H170L, CF-H180AI, CF-H180AL, CF-H180DI, CF-H180DL, CF-H190I, CF-H190L, CF-HQ190I, CF-HQ190L, CF-LV1I, CF-LV1L, CF-Q150I, CF-Q150L, CF-Q160S, CF-Q180AI, CF-Q180AL. 510(k) Numbers: K954451, K112680, K100584, K051645, K111756, K001241, K911278.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FET·September 25, 2023