Skip to content

Oncobionics, Inc.

United StatesFDA applicant, unverified

Devices
2

What Oncobionics, Inc. makes

Oncobionics, Inc. manufactures the OncoBionic System, a medical device designed for intraoperative imaging and guidance during surgical procedures. The system includes variations such as the OncoBionic System with 6 Probe Output, which appears to support expanded imaging capabilities for targeted tissue assessment.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. Oncobionics, Inc. is based in the United States.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Oncobionic System Ref K060054

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Oncobionic System With 6 Probe Output Ref K080202

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

Frequently asked questions

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

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

Which registries list Oncobionics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Oncobionics, Inc. include ONCOBIONIC SYSTEM and ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT.

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