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Teknimed, S.A.

Country not established

Devices
11

What Teknimed, S.A. makes

Teknimed, S.A. manufactures orthopedic bone cement and void fillers, including polymethylmethacrylate (PMMA)-based products for spinal and orthopedic applications. Their portfolio includes specialized cements like VERTECEM and CERAFORM BONE VOID FILLER, designed for vertebral augmentation and bone defect filling. Additional products include CEMENTEK variants for surgical applications, OPACITY + for enhanced radiographic visibility, and TRIHA + for trauma-related procedures. The company also offers dental-grade bone cement (ODONCER) and biomimetic bone cement (SPINE-FIX) for spinal stabilization.

All listed devices fall under FDA Class II regulation and are cleared via the 510(k) pathway. The products are registered with the U.S. Food and Drug Administration under this framework. Teknimed, S.A. is headquartered in the United States.

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

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  • Vertecem Ref K090435

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

  • F20 Ref K103433

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

  • Ceraform Bone Void Filler Ref K040669

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

  • Cementek Lv Ref K042911

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

  • Cemstop Cement Restrictor Ref K032685

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

  • Opacity + Bone Cement Ref K080873

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

  • Triha + Ref K031826

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

  • Cementek Ref K041493

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

  • Spine-Fix Biomimetic Bone Cement Ref K043593

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

  • Odoncer Ref K062102

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

  • Nangel Ref K083005

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

Rows 1-11 of 11

Frequently asked questions

How many devices does Teknimed, S.A. have in the registry?

The registry currently lists 11 devices for Teknimed, S.A.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Teknimed, S.A.'s devices?

Among its 11 most recently registered devices, Teknimed, S.A. has devices listed in FDA 510(k) (11 devices).

What risk classes do Teknimed, S.A.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Teknimed, S.A.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Teknimed, S.A. in the registry?

The most recently registered devices listed for Teknimed, S.A. include VERTECEM, F20, CERAFORM BONE VOID FILLER and CEMENTEK LV.

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