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Medigus, Ltd.

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Medigus, Ltd. is a medical device manufacturer, with 7 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) as of 14 Nov 2026.

Devices
7

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA 510(k) 4
  • FDA GUDID 3

A device listed in two registries counts in both.

Device classes
  • FDA Class II 7
Identifiers
  • DUNS 532281169

What Medigus, Ltd. makes

Medigus manufactures endoscopic stapling systems, including manual linear staplers and non-cutting staple loading units for minimally invasive surgical procedures. Their portfolio includes dedicated cartridge systems like the MUSE Staple Cartridge and the SRS Endoscopic Stapling System, designed for precise tissue approximation and division. The company also produces general-purpose ultrasound imaging consoles, such as the MUSE Console, for intraoperative visualization.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI databases. These products are intended for surgical applications and are subject to premarket notification requirements.

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

Catalogue7

Newest first, rows 1-7 of 7

  • MUSE Staple Cartridge 02

    Listed Registry: GUDID Class:II
  • MUSE Endostapler 01

    Listed Registry: GUDID Class:II
  • MUSE Console 01

    Listed Registry: GUDID Class:II
  • Srs Endoscopic Stapling System Ref K132151

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Srs Endoscopic Stapling System Ref K120299

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • MUSE System Ref K143634

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • MUSE System Ref K151001

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

Company details

DUNS number
532281169
Phone
+972543516320

Frequently asked questions

How many devices does Medigus, Ltd. have in the registry?

The registry currently lists 7 devices for Medigus, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medigus, Ltd.'s devices?

Among its 7 most recently registered devices, Medigus, Ltd. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Medigus, Ltd.'s devices fall under?

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

What are the newest devices from Medigus, Ltd. in the registry?

The most recently registered devices listed for Medigus, Ltd. include MUSE Staple Cartridge 02, MUSE Endostapler 01, MUSE Console 01 and SRS ENDOSCOPIC STAPLING SYSTEM.

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