BEUDAMED
    111 results · 12ms · 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 Status: Terminated ×

    37% Etching Gel-3ml syringe, part #N01H The intended use of these devices is to etch tooth dentin/enamel in order to prepare the tooth surface prior to the application of a bonding agent.

    FDA Recall
    Terminated ·Kerr/pentron Dba Kerr Corporation And Pentron Clinical·Product code EBF·March 31, 2011

    PREMISE, PART NO. 34086, 10 PACK UNIDOSE PREMISE A2 SAMPLE, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32674, 10 PACK UNIDOSE PREMISE C2 OPAQUE, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32812, 10 PACK UNIDOSE PREMISA A2 (INTERNATIONAL ONLY), dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32677, 10 PACK UNIDOSE PREMISE TRANS GREY, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    Heliomolar Refill 20x0.25g 210/A3, Product code 541503AN, Catalog number 541503

    FDA Recall
    Terminated ·Ivoclar Vivadent, Inc.·Product code EBF·August 3, 2017

    PREMISE KIT, PART NO. 32612, UNIDOSE PREMISE MASTER KIT, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32814, 10 PACK UNIDOSE PREMISA A3.5 (INTERNATIONAL ONLY), dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32837, 10 PACK UNIDOSE PREMISA TRANSLUCENT AMBER (INTERNATIONAL ONLY), dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32822, 10 PACK UNIDOSE PREMISA C3 (INTERNATIONAL ONLY), dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32672, 10 PACK UNIDOSE PREMISE B1 OPAQUE, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32664, 10 PACK UNIDOSE PREMISE D3, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    37% Etching Gel-1ml syringe 50 pk, part # T06B The intended use of these devices is to etch tooth dentin/enamel in order to prepare the tooth surface prior to the application of a bonding agent.

    FDA Recall
    Terminated ·Kerr/pentron Dba Kerr Corporation And Pentron Clinical·Product code EBF·March 31, 2011

    Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling small class I cavities and extended fissure sealing - Filling class II - V cavities including V-shaped defects and cervical caries - Blocking out undercuts - Lining or coating cavities - Repairing fillings and veneers - Luting translucent prosthetic pieces (e.g., full ceramic crowns, etc.).

    FDA Recall
    Terminated ·Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany·Product code EBF·July 9, 2019

    PREMISE, PART NO. 32666, 10 PACK UNIDOSE PREMISE XL1, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32676, 10 PACK UNIDOSE PREMISE TRANS AMBER, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32669, 10 PACK UNIDOSE PREMISE A3 OPAQUE, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32650, 10 PACK UNIDOSE PREMISE A1, dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    PREMISE, PART NO. 32824, 10 PACK UNIDOSE PREMISA D2 (INTERNATIONAL ONLY), dental composite

    FDA Recall
    Terminated ·Kerr Corp·Product code EBF·September 5, 2008

    Flow Tec Nano-Hybrid Flowable Affected Product Syringe Part No. Value Pack Part. No. Shade BEN3784-514 BEN3786-754 A1 BEN3784-532 BEN3786-763 A2 BEN3784-541 BEN3784-738 A3 BEN3784-550 BEN3784-747 A3.5 BEN3784-569 BEN3784-756 A4 BEN3784-578 BEN3784-765 B1 BEN3784-596 BEN3784-774 B2 BEN3784-603 BEN3784-783 C1 BEN3784-612 BEN3784-792 C2 BEN3784-621 BEN3784-809 C3 BEN3784-649 BEN3784-818 D2 BEN3784-722 BEN3784-818 Universal Opaque BEN3784-685 BEN3784-827 A0 BEN3784-701 BEN3784-836 Incisal. The intended use of this device is as a light cured, low viscosity, hybrid composite material which is compatible with a variety of bonding agents and luting materials during the course of dental restorations. Artiste Flowable and Flow Tec (private label of Artiste Flowable) are indicated for restorations of carious lesions, porcelain repairs, small core build-ups, fill-in of surface enamel irregularities, etc.

    FDA Recall
    Terminated ·Sybron Dental Specialties·Product code EBF·March 3, 2011