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Pacira Biosciences, Inc.

United StatesFDA applicant, unverified

Devices
2

What Pacira Biosciences, Inc. makes

Pacira Biosciences, Inc. manufactures the iovera System and iovera° System, which are medical devices designed for minimally invasive procedures, including nerve block applications.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • iovera System Ref K220656

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • iovera° System Ref K243677

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

Frequently asked questions

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

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

Which registries list Pacira Biosciences, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Pacira Biosciences, Inc. include iovera System and iovera° System.

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