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Ncontact Surgical, Inc.

United StatesFDA applicant, unverified

Devices
7

What Ncontact Surgical, Inc. makes

Ncontact Surgical, Inc. manufactures coagulation systems and guided coagulation devices, including the NUMERIS and EPI-SENSE series with integrated VISITRAX imaging. These systems are designed for precise tissue coagulation in surgical applications, with models differentiated by features such as guided visualization and kit configurations. The portfolio includes standalone coagulation devices and bundled kits for procedural use.

The company’s coagulation devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) database, reflecting their regulatory clearance for commercial distribution in the United States. The manufacturer is based in the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Ncontact Surgical, Inc. have in the registry?

The registry currently lists 7 devices for Ncontact Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ncontact Surgical, Inc.'s devices?

Among its 7 most recently registered devices, Ncontact Surgical, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Ncontact Surgical, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Ncontact Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ncontact Surgical, Inc. in the registry?

The most recently registered devices listed for Ncontact Surgical, Inc. include NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125, NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025, NCONTACT COAGULATION SYSTEM KIT, MODEL CSK and EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX.

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