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American Surgical Technologies Corp.

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Devices
1

What American Surgical Technologies Corp. makes

American Surgical Technologies Corp. manufactures the 3DSCOPE, a device designed for enhanced visualization in surgical procedures, providing three-dimensional imaging to improve precision and depth perception during operations.

The 3DSCOPE is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • 3DSCOPE Ref K923160

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

Frequently asked questions

How many devices does American Surgical Technologies Corp. have in the registry?

The registry currently lists 1 device for American Surgical Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list American Surgical Technologies Corp.'s devices?

Among its 1 most recently registered device, American Surgical Technologies Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do American Surgical Technologies Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for American Surgical Technologies Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from American Surgical Technologies Corp. in the registry?

The most recently registered devices listed for American Surgical Technologies Corp. include 3DSCOPE.

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