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Silent Call Corp.

United StatesFDA applicant, unverified

Devices
2

What Silent Call Corp. makes

Silent Call Corp. manufactures medical alert devices designed for personal safety and emergency communication. Their product line includes the MED-A-CALL Assist Device and the Personal Alert Assist Device, which are intended to enable users to summon help discreetly in medical or home settings.

These devices are regulated under the FDA’s 510(k) clearance process, with some classified as Class I and others as Class II. They are listed in the FDA’s 510(k) registry and are intended for distribution in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Med-A-Call Assist Device Ref K890596

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Personal Alert Assist Device Ref K890445

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

Frequently asked questions

How many devices does Silent Call Corp. have in the registry?

The registry currently lists 2 devices for Silent Call Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Silent Call Corp.'s devices?

Among its 2 most recently registered devices, Silent Call Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Silent Call Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Silent Call Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Silent Call Corp. in the registry?

The most recently registered devices listed for Silent Call Corp. include MED-A-CALL ASSIST DEVICE and PERSONAL ALERT ASSIST DEVICE.

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