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Sea-Band UK, Ltd.

United KingdomFDA applicant, unverified

Devices
1

What Sea-Band UK, Ltd. makes

Sea-Band UK, Ltd. manufactures the SEA-BAND, a wristband designed to provide wrist acupuncture pressure for motion sickness relief and nausea management.

The SEA-BAND is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Sea-Band Ref K033268

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

Frequently asked questions

How many devices does Sea-Band UK, Ltd. have in the registry?

The registry currently lists 1 device for Sea-Band UK, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sea-Band UK, Ltd.'s devices?

Among its 1 most recently registered device, Sea-Band UK, Ltd. has devices listed in FDA 510(k) (1 device).

What are the newest devices from Sea-Band UK, Ltd. in the registry?

The most recently registered devices listed for Sea-Band UK, Ltd. include SEA-BAND.

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