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Cognifisense, Inc.

United StatesFDA applicant, unverified FDA FEI 3042903607

Devices
2
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue2

Newest first, rows 1-2 of 2

  • Vrnt Ref K230814

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Vrnt Ref K254004

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

Company details

FDA FEI number
3042903607
Address
1271 Lakeside Dr Apt 3121, Sunnyvale, CA, 94085

Frequently asked questions

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

The registry currently lists 2 devices for Cognifisense, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cognifisense, Inc.'s devices?

Among its 2 most recently registered devices, Cognifisense, Inc. has devices listed in FDA 510(k) (2 devices).

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

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

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

The most recently registered devices listed for Cognifisense, Inc. include VRNT.

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