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Kerber Usa Inc.

Country not established FDA establishment FEI 3017419219

Devices
6
Registrations
FDA
FDA recalls
0

Catalogue6

Newest first, rows 1-6 of 6

Company details

FDA FEI number
3017419219
Address
1576 Sweet Home Rd, Amherst, NY, 14228

Frequently asked questions

How many devices does KERBER USA INC. have in the registry?

The registry currently lists 6 devices for KERBER USA INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list KERBER USA INC.'s devices?

Among its 6 most recently registered devices, KERBER USA INC. has devices listed in FDA GUDID (6 devices).

What risk classes do KERBER USA INC.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for KERBER USA INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from KERBER USA INC. in the registry?

The most recently registered devices listed for KERBER USA INC. include SunPowerLED SuperPalm 1050, SunPowerLED Palm Ultimate, SunPowerLED Palm Professional and SunPowerLED Mini-Canopy.

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.