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Exeter Instruments, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Exeter Instruments, Inc. makes

Exeter Instruments, Inc. manufactures operating loupes used for surgical visualization.

The company is based in the United States, and its products are classified as Class I devices listed in the FDA 510(k) registry.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Exeter Operating Loupe Ref K810817

    Class I
    Active 510(k) 510(k) I
  • Exeter Operating Loupe Ref K863983

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

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

Which registries list Exeter Instruments, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Exeter Instruments, Inc. include EXETER OPERATING LOUPE.

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