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Remedent NV

Country not established

Devices
2

What Remedent NV makes

Remedent NV manufactures medical devices including the REMECURE Model CL 15E, a device designed for wound care and tissue treatment, and the REMESENSE system, which appears to monitor or assess biological responses in wound healing environments.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Remecure Model Cl 15E Ref K023652

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Remesense Ref K082594

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

Frequently asked questions

How many devices does Remedent NV have in the registry?

The registry currently lists 2 devices for Remedent NV. Devices recorded under merged duplicate company entries are counted once.

Which registries list Remedent NV's devices?

Among its 2 most recently registered devices, Remedent NV has devices listed in FDA 510(k) (2 devices).

What risk classes do Remedent NV's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Remedent NV's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Remedent NV in the registry?

The most recently registered devices listed for Remedent NV include REMECURE MODEL CL 15E and REMESENSE.

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