Skip to content

Jeneric/Pentron, Inc.

United StatesFDA applicant, unverified

Devices
78
FDA recalls
1

What Jeneric/Pentron, Inc. makes

Jeneric/Pentron, Inc. manufactures dental restorative and prosthetic materials, including crown and bridge composite systems, dual-cure activators, dental glazes and sealants, casting alloys, core posts, and light-curing units. Specific products include the Conquest C&B VLC Glaze/Sealant, Bond-It Dual Cure Activator, Jewel Cast III, Nugold 2%, Avante Curelight, Gold Core Post Solder, Build-It FR, and Procom.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Jeneric/Pentron, Inc. is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue78

Newest first, rows 51-78 of 78

Search and filter all 78 devices
Skip device list

  • KB40-Kf Ref K922956

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cosmic Ref K010044

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Opc Low Wear Opaque Porcelain Ref K993249

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Conquest Smooth Touch Ref K941377

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Q3 (Light And Universal) Impression Material Ref K923202

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dentin Conditioning And Adhesive (Bond 1) Ref K973388

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Opc 3g All-Ceramic System, Core And Overlay Porcelains Ref K994435

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Conquest Senior Ref K941376

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Rx Everest Ref K001051

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dentin Conditioning And Adhesive System Ref K936222

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bond 1 C & B Ref K994359

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Gold Core 75 Ref K993175

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Conquest Direct Filling Composite (Dfc) Ref K904724

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Quell Desensitizer Ref K010957

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bond-3 Adhesive Ref K020499

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Gold Core Ii Ref K003039

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bio C & B Ref K926146

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Alert Ref K974131

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Avante Micro Crystal System Ref K012231

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bond-1 C & B Ref K013543

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Sculpture Flow Ref K001623

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adhesive, Bracket And Tooth Conditioner Resin Ref K921283

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • R2+ Ref K934758

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Rx G-Universal Ref K000360

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Comp=flow Ref K952662

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dentin Conditioning And Adhesive System (Bond-1) Ref K013542

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fiberlite, Fiberlite Hs And Fiberseal Ref K884038

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Zenon Plus Ref K922955

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 51-78 of 78

Showing 51-78 of 78

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by Jeneric/Pentron, Inc., initiated on 2009-10-22. By recorded status: 1 terminated. The reasons filed fall into these groups: packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2009

    • 22 Oct 2009 Z-0482-2010 Unclassified (pre-2012) Terminated Pentron Clinical Technologies LLC received two (2) complaints alleging that the TempSpan Dual-Cure Temporary Crown and Bridge Material was not setting. Investigation of product in inventory was conducted and it was confirmed that some of the bottles had been mispackaged with an incorrect catalyst. Distribution: Nationwide Submission number: K021457