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Aesculap-Meditec North America

Country not established

Devices
6

What Aesculap-Meditec North America makes

The company manufactures slit lamp examination devices, including the SL07 and SL08 models, for ophthalmic diagnostics. It also produces YAG laser systems, such as the Dermablate ER and MCL 29, for ocular procedures. Additional offerings include ruby and Nd:YAG laser systems, like the Rubystar with Q-switch and Mediostar H, with some models featuring skin cooling attachments. A laser control interface, Meditec Link, is included for system management.

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.

Catalogue6

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Frequently asked questions

How many devices does Aesculap-Meditec North America have in the registry?

The registry currently lists 6 devices for Aesculap-Meditec North America. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aesculap-Meditec North America's devices?

Among its 6 most recently registered devices, Aesculap-Meditec North America has devices listed in FDA 510(k) (6 devices).

What risk classes do Aesculap-Meditec North America's devices fall under?

Among its 6 most recently registered devices, the classes recorded for Aesculap-Meditec North America's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aesculap-Meditec North America in the registry?

The most recently registered devices listed for Aesculap-Meditec North America include AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08, DERMABLATE ER: YAG LASER SYSTEM, MEDITEC LINK and LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE.

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