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Local Silence, Inc.

Country not established

Devices
1

What Local Silence, Inc. makes

Local Silence, Inc. manufactures the Silent Night I, a device designed to reduce noise in medical environments, such as patient rooms or critical care units, to improve sleep quality and patient recovery.

The Silent Night I is classified as a Class II medical device in the US and is listed under FDA 510(k) clearance. 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

  • Silent Night I Ref K963597

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

Frequently asked questions

How many devices does Local Silence, Inc. have in the registry?

The registry currently lists 1 device for Local Silence, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Local Silence, Inc.'s devices?

Among its 1 most recently registered device, Local Silence, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Local Silence, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Local Silence, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Local Silence, Inc. in the registry?

The most recently registered devices listed for Local Silence, Inc. include SILENT NIGHT I.

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