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Fertility Instrumentation, Inc.

Country not established

Devices
1

What Fertility Instrumentation, Inc. makes

Fertility Instrumentation, Inc. makes endocervical aspirators, which are medical devices used to collect tissue or fluid samples from the endocervical canal for diagnostic purposes.

The company's endocervical aspirators are classified as Class II devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Endocervical Aspirator Ref K812175

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

Frequently asked questions

How many devices does Fertility Instrumentation, Inc. have in the registry?

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

Which registries list Fertility Instrumentation, Inc.'s devices?

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

What risk classes do Fertility Instrumentation, Inc.'s devices fall under?

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

What are the newest devices from Fertility Instrumentation, Inc. in the registry?

The most recently registered devices listed for Fertility Instrumentation, Inc. include ENDOCERVICAL ASPIRATOR.

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