Skip to content

Pentron Clinical Technologies

Country not established

Devices
13

What Pentron Clinical Technologies makes

Pentron Clinical Technologies makes dental materials and equipment including fiber-reinforced composite fillers (FIBERFILL SGP, FIBERFILL AGP), flowable composites (SIMILE FLOW, ARTISTE SE FLOWABLE COMPOSITE), adhesive systems (GENERATION 8 SE ADHESIVE, RM BOND, NANO-BOND II ADHESIVE SYSTEM), root canal sealants (SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE), curing units (AVANTE LED CURING UNIT, MODEL N44, BUILD-IT LIGHT CURE), and all-purpose cement (CEMENT-IT ALL PURPOSE, MODEL N97).

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

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

Search and filter all 13 devices
Skip device list

  • Fiberfill Sgp Ref K023819

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

  • Trionomer Ref K022150

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

  • Fiberfill Agp Ref K023818

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

  • Se Epiphany Root Canal Sealant, Model N59SE Ref K060889

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

  • Avante Led Curing Unit, Model N44 Ref K052349

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

  • Generation 8 Se Adhesive Ref K072480

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

  • Rm Bond, Model J032 Ref K072830

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

  • Simile Flow Ref K052106

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

  • Artiste Se Flowable Composite, Model N280 Ref K072545

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

  • Build-It Light Cure Ref K091512

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

  • Nano-Bond Ii Adhesive System Ref K071500

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

  • Cement-It All Purpose, Model N97 Ref K060698

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

  • Lute-It Ii Veneer Cement, Model NO6 Ref K081887

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Pentron Clinical Technologies have in the registry?

The registry currently lists 13 devices for Pentron Clinical Technologies. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pentron Clinical Technologies's devices?

Among its 13 most recently registered devices, Pentron Clinical Technologies has devices listed in FDA 510(k) (13 devices).

What risk classes do Pentron Clinical Technologies's devices fall under?

Among its 13 most recently registered devices, the classes recorded for Pentron Clinical Technologies's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pentron Clinical Technologies in the registry?

The most recently registered devices listed for Pentron Clinical Technologies include FIBERFILL SGP, TRIONOMER, FIBERFILL AGP and SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE.

Generated automatically from registry data and not verified by a human reviewer.