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Hanuri Distribution, Inc

United Statesfrom the FDA registration address FDA establishment FEI 3007778244

Devices
2
Registrations
FDA
FDA recalls
0

Catalogue2

Newest first, rows 1-2 of 2

  • Powerpress Unit Ref K110276

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Powerpress Recovery Unit Ref K202044

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

Company details

FDA FEI number
3007778244
Address
9601 Owensmouth Ave Ste 8, Chatsworth, CA, 91311

Frequently asked questions

How many devices does HANURI DISTRIBUTION, INC have in the registry?

The registry currently lists 2 devices for HANURI DISTRIBUTION, INC. Devices recorded under merged duplicate company entries are counted once.

Which registries list HANURI DISTRIBUTION, INC's devices?

Among its 2 most recently registered devices, HANURI DISTRIBUTION, INC has devices listed in FDA 510(k) (2 devices).

What risk classes do HANURI DISTRIBUTION, INC's devices fall under?

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

What are the newest devices from HANURI DISTRIBUTION, INC in the registry?

The most recently registered devices listed for HANURI DISTRIBUTION, INC include POWERPRESS UNIT and Powerpress Recovery Unit.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.