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Wilde-USA, Inc.

United StatesFDA applicant, unverified

Devices
16

What Wilde-USA, Inc. makes

Wilde-USA, Inc. manufactures dental restorative and prosthetic materials, including amalgam alloys such as Keralloy Non-Gamma 2 and Keralloy-D Caps, adhesive bonding systems like the Wilde Adhesive Bonding System, light-curing composite resins, casting alloys (Wil-PDS & Wil-PDI), denture teeth (Planustar and Dens Nobilis), orthodontic materials (Wil-O-Dont/WIL-O-LUX), and related products such as Conversil FL and P, Compasep, Keramail, and Compacolor.

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

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue16

Newest first, rows 1-16 of 16

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  • Keralloy Non-Gamma 2 Amalgam Ref K912992

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

  • Conversil Fl And Conversil P Ref K913583

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

  • Wilde Adhesive Bonding System Ref K913581

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

  • Planustar And Dens Nobilis Denture Teeth Ref K912989

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

  • Wil-Pds & Wil-Pdi Casting Alloys Ref K915250

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

  • Wilde Light Curing Composite Restorative Resins Ref K913089

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

  • Wil-O-Dont Orthodontic Material/Wil-O-Lux Ref K920557

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

  • Compatit R Ref K913582

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

  • Keralloy-D Caps Ref K915654

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

  • Compasep Ref K920649

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

  • Keramail Ref K915653

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

  • Compacolor Ref K923472

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

  • Wilde Auxiliaries Ref K912991

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

  • Compalux Stroboscopic Light Polymerization Device Ref K912994

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

  • Converbase Ref K912990

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

  • Wilde Denture Resins Ref K912993

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

Rows 1-16 of 16

Frequently asked questions

How many devices does Wilde-USA, Inc. have in the registry?

The registry currently lists 16 devices for Wilde-USA, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Wilde-USA, Inc.'s devices?

Among its 16 most recently registered devices, Wilde-USA, Inc. has devices listed in FDA 510(k) (16 devices).

What risk classes do Wilde-USA, Inc.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Wilde-USA, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Wilde-USA, Inc. in the registry?

The most recently registered devices listed for Wilde-USA, Inc. include KERALLOY NON-GAMMA 2 AMALGAM, CONVERSIL FL AND CONVERSIL P, WILDE ADHESIVE BONDING SYSTEM and PLANUSTAR AND DENS NOBILIS DENTURE TEETH.

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