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Odyssey Medical, Inc.

United StatesFDA applicant, unverified

Devices
4

What Odyssey Medical, Inc. makes

Odyssey Medical, Inc. manufactures medical devices including flow controllers for vascular applications, punctual occluders for ophthalmic procedures, and LASIK eye drapes designed for sterile surgical use.

The company’s portfolio comprises Class II and Unclassified (U) devices, with products listed via FDA 510(k) clearance. The manufacturer is based in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

  • Flow Controller Ref K090938

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Punctual Occluder Ref K972523

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Punctual Occluder Ref K970631

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Lasik Eye Drape Ref K042977

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

Frequently asked questions

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

The registry currently lists 4 devices for Odyssey Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Odyssey Medical, Inc.'s devices?

Among its 4 most recently registered devices, Odyssey Medical, Inc. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for Odyssey Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Odyssey Medical, Inc. include FLOW CONTROLLER, PUNCTUAL OCCLUDER and LASIK EYE DRAPE.

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