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Galileo Electro-Optics Corp.

United StatesFDA applicant, unverified

Devices
7

What Galileo Electro-Optics Corp. makes

Galileo Electro-Optics Corp. manufactures reusable and disposable endoscopes, including hysteroscopes, laparoscopes, and arthroscopes, designed for minimally invasive surgical procedures. Their products are used in gynecological, orthopedic, and general surgical applications, providing visual access to internal body cavities and joints. The company also supplies disposable endoscopes for single-use procedures, reducing infection risks and streamlining workflows in operating rooms.

The company’s devices fall under FDA Class II regulation, requiring premarket notification (510(k)) clearance before commercial distribution in the US. These products are listed in the FDA’s 510(k) database, reflecting their authorised status for sale under US regulatory requirements. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

  • Galileo Hysteroscopes And Laparoscopes Ref K962256

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Arthroscopes Ref K936280

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Endoscopes Ref K936279

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Arthroscopes Ref K934707

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Endoscopes Ref K934649

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Endoscopes Ref K962116

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Galileo Disposable Endoscopes Ref K981928

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

Frequently asked questions

How many devices does Galileo Electro-Optics Corp. have in the registry?

The registry currently lists 7 devices for Galileo Electro-Optics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Galileo Electro-Optics Corp.'s devices?

Among its 7 most recently registered devices, Galileo Electro-Optics Corp. has devices listed in FDA 510(k) (7 devices).

What risk classes do Galileo Electro-Optics Corp.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Galileo Electro-Optics Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Galileo Electro-Optics Corp. in the registry?

The most recently registered devices listed for Galileo Electro-Optics Corp. include GALILEO HYSTEROSCOPES AND LAPAROSCOPES, GALILEO ARTHROSCOPES, GALILEO ENDOSCOPES and GALILEO DISPOSABLE ENDOSCOPES.

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