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Kay Elemetrics Corp.

United StatesFDA applicant, unverified

Devices
5

What Kay Elemetrics Corp. makes

Kay Elemetrics Corp. manufactures diagnostic and procedural devices for laryngology, otolaryngology, and swallowing assessment, including rigid telescopic endoscopes, digital video recording systems, and laryngopharyngeal stroboscopes. Their products also include electroglottography systems for vocal fold analysis and swallowing workstations for clinical evaluation of dysphagia. These tools are designed for use in clinical examinations and research settings.

The company’s portfolio includes devices classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance database. Products are intended for use in the United States and comply with applicable medical device regulations. The manufacturer is based in the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Kay Elemetrics Corp. have in the registry?

The registry currently lists 5 devices for Kay Elemetrics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kay Elemetrics Corp.'s devices?

Among its 5 most recently registered devices, Kay Elemetrics Corp. has devices listed in FDA 510(k) (5 devices).

What risk classes do Kay Elemetrics Corp.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Kay Elemetrics Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kay Elemetrics Corp. in the registry?

The most recently registered devices listed for Kay Elemetrics Corp. include ELECTROGLOTTOGRAPH, 9105 RIGID TELESCOPIC ENDOSCOPE, DIGITAL VIDEO RECORDING SYSTEM and RLS 9100 RHINO-LARYNGEAL STROBOSCOPE.

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