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Mesynthes, Ltd.

Country not established

Devices
2

What Mesynthes, Ltd. makes

Mesynthes, Ltd. manufactures customizable dermal and dental templates, including the ENDOFORM DERMAL TEMPLATE and ENDOFORM DENTAL TEMPLATE, designed for surgical planning and patient-specific applications.

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

  • Endoform Dermal Template Ref K092096

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

  • Endoform Dental Template Ref K101546

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

Frequently asked questions

How many devices does Mesynthes, Ltd. have in the registry?

The registry currently lists 2 devices for Mesynthes, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mesynthes, Ltd.'s devices?

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

What are the newest devices from Mesynthes, Ltd. in the registry?

The most recently registered devices listed for Mesynthes, Ltd. include ENDOFORM DERMAL TEMPLATE and ENDOFORM DENTAL TEMPLATE.

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