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Asahi Intecc USA, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3004718255

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3004718255
Address
3002 Dow Ave Suite 212, Tustin, CA, 92780

Frequently asked questions

How many devices does ASAHI INTECC USA, INC. have in the registry?

The registry currently lists 1 device for ASAHI INTECC USA, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ASAHI INTECC USA, INC.'s devices?

Among its 1 most recently registered device, ASAHI INTECC USA, INC. has devices listed in FDA 510(k) (1 device).

What risk classes do ASAHI INTECC USA, INC.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for ASAHI INTECC USA, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from ASAHI INTECC USA, INC. in the registry?

The most recently registered devices listed for ASAHI INTECC USA, INC. include ASAHI TREASURE FLOPPY PERIPHERAL GUIDE WIRE.

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.