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Key Tronic Corp.

Country not established FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Key Tronic Corp. makes

Key Tronic Corp. manufactures the APOLLO Heart Rate Indicator, a device designed to display real-time heart rate data for monitoring purposes.

The APOLLO Heart Rate Indicator is classified as a Class II medical device and is listed under FDA’s 510(k) regulatory pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Apollo Heart Rate Indicator Ref K791207

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

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Key Tronic Corporation Juarez Chihuahua · MX FEI 3027285900

Frequently asked questions

How many devices does Key Tronic Corp. have in the registry?

The registry currently lists 1 device for Key Tronic Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Key Tronic Corp.'s devices?

Among its 1 most recently registered device, Key Tronic Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Key Tronic Corp.'s devices fall under?

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

What are the newest devices from Key Tronic Corp. in the registry?

The most recently registered devices listed for Key Tronic Corp. include APOLLO HEART RATE INDICATOR.

Which FDA establishments are linked to Key Tronic Corp.?

1 FDA establishment is linked to Key Tronic Corp. in the registry; they are listed on the company page.

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