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Jurgan Development & Mfg., Ltd.

United Statesfrom the FDA registration address FDA establishment FEI 2183463

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

  • Jurgan Pin Ball Ref K831072

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

Company details

FDA FEI number
2183463
Address
6018 SOUTH HIGHLANDS AVE., MADISON, WI, 53705

Frequently asked questions

How many devices does JURGAN DEVELOPMENT & MFG., LTD. have in the registry?

The registry currently lists 1 device for JURGAN DEVELOPMENT & MFG., LTD.. Devices recorded under merged duplicate company entries are counted once.

Which registries list JURGAN DEVELOPMENT & MFG., LTD.'s devices?

Among its 1 most recently registered device, JURGAN DEVELOPMENT & MFG., LTD. has devices listed in FDA 510(k) (1 device).

What risk classes do JURGAN DEVELOPMENT & MFG., LTD.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for JURGAN DEVELOPMENT & MFG., LTD.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from JURGAN DEVELOPMENT & MFG., LTD. in the registry?

The most recently registered devices listed for JURGAN DEVELOPMENT & MFG., LTD. include JURGAN PIN BALL.

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.