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Tumble Forms, Inc.

Also registered as Tumble Forms

United Statesfrom the FDA registration address FDA establishment FEI 1000119616

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

  • Tumble Forms Tristander Ref K922965

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

Company details

FDA FEI number
1000119616
Address
1013 BARKER RD., DOLGEVILLE, NY, 11329

Frequently asked questions

How many devices does TUMBLE FORMS, INC. have in the registry?

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

Which registries list TUMBLE FORMS, INC.'s devices?

Among its 1 most recently registered device, TUMBLE FORMS, INC. has devices listed in FDA 510(k) (1 device).

What risk classes do TUMBLE FORMS, INC.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for TUMBLE FORMS, INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from TUMBLE FORMS, INC. in the registry?

The most recently registered devices listed for TUMBLE FORMS, INC. include TUMBLE FORMS TRISTANDER.

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.