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Pentron Corp.

United StatesFDA applicant, unverified

Devices
15

What Pentron Corp. makes

Pentron Corp. manufactures dental materials and systems, including radiopaque resin-based restorative materials (e.g., C-17, NUMBER 21 R/R SYSTEM), temporary crown and bridge materials (FLEX SPAN), pit and fissure sealants (C-22), and adhesive dentin materials (CODE #23 R SYSTEM). The portfolio also includes supplementary kits for staining and characterization (OPTEC kits) and dual-cure radiopaque composites.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Pentron Corp. is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue15

Newest first, rows 1-15 of 15

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  • C-17 Ref K841268

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

  • Number 21 R/R System Ref K841457

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

  • #24L System Ref K873878

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

  • Number 20 R/L System Ref K841458

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

  • Pentra-Fil Ii Ref K840727

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

  • Dual-Cure Radiopaque Ref K874189

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

  • C-18 Ref K841267

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

  • Optec Supplementary Kit Ref K874275

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

  • Flex Span Temporary Crown & Bridge Material Ref K021457

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

  • Code #23 R System (Dentin Adhesive Material) Ref K873683

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

  • Optec Stain Characterization And Modification Kit Ref K874162

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

  • C-22 Pit & Fissure Sealant Ref K844057

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

  • C-19 Ref K841269

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

  • Chameleon Bonding Kit Ref K854803

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

  • Pentron High Strength Porcelain Ref K864404

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

Rows 1-15 of 15

Frequently asked questions

How many devices does Pentron Corp. have in the registry?

The registry currently lists 15 devices for Pentron Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pentron Corp.'s devices?

Among its 15 most recently registered devices, Pentron Corp. has devices listed in FDA 510(k) (15 devices).

What risk classes do Pentron Corp.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for Pentron Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pentron Corp. in the registry?

The most recently registered devices listed for Pentron Corp. include C-17, NUMBER 21 R/R SYSTEM, #24L SYSTEM and NUMBER 20 R/L SYSTEM.

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