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Dilon Medical Technologies, Ltd.

Also registered as DILON MEDICAL TECHNOLOGIES, Inc

Country not established FDA

Devices
5
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Dilon Medical Technologies, Ltd. makes

Dilon Medical Technologies specializes in intraoperative tumour margin analysis probes designed to assist surgeons in identifying cancerous tissue during operations. Their devices include handheld probes and console systems that provide real-time feedback to help determine surgical margins accurately.

The company’s products are classified as Class III medical devices under FDA regulations and are listed under both Premarket Approval (PMA) and Unique Device Identification (UDI) programs. The manufacturer operates from the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Company details

DUNS number
600832361

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Dilon Medical Technologies Ltd. Caesarea Haifa · IL FEI 3005755031

Frequently asked questions

How many devices does Dilon Medical Technologies, Ltd. have in the registry?

The registry currently lists 5 devices for Dilon Medical Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dilon Medical Technologies, Ltd.'s devices?

Among its 5 most recently registered devices, Dilon Medical Technologies, Ltd. has devices listed in EUDAMED (2 devices), FDA PMA (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Dilon Medical Technologies, Ltd.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Dilon Medical Technologies, Ltd.'s devices are Class III. Each device page shows its own class and authorisation.

What are the newest devices from Dilon Medical Technologies, Ltd. in the registry?

The most recently registered devices listed for Dilon Medical Technologies, Ltd. include MarginProbe® Probe AC0600001, Margin Probe Console 2.0 SA0590040, Margin Probe Console 1.2R SA0590020 and MarginProbe® Probe AC0300001.

Which FDA establishments are linked to Dilon Medical Technologies, Ltd.?

1 FDA establishment is linked to Dilon Medical Technologies, Ltd. in the registry; they are listed on the company page.

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