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Ascend Eagle, Inc.

United StatesFDA applicant, unverified FDA FEI 3003243726

Devices
3
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue3

Newest first, rows 1-3 of 3

Company details

FDA FEI number
3003243726
Address
828 San Pablo Avenue, Pinole, CA, 94564

Frequently asked questions

How many devices does Ascend Eagle, Inc. have in the registry?

The registry currently lists 3 devices for Ascend Eagle, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ascend Eagle, Inc.'s devices?

Among its 3 most recently registered devices, Ascend Eagle, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Ascend Eagle, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Ascend Eagle, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Ascend Eagle, Inc. in the registry?

The most recently registered devices listed for Ascend Eagle, Inc. include NON STERILE POWDER-FREE, NATURAL OR AQUA LANO-E NITRILE EXAMINATION GLOVES, WITH OR WITHOUT CITRUS/ PEPPERMINT SCENT, NON-STERILE POWDER FREE NATURAL/GREEN LANO-E LATEX EXAM GLOVES, WITH OR WIHOUT CITRUS/PEPPERMINT SCENT PLUS A PROTEIN and NON-STERILE POWDER- FREE PEACH COLOR, NITRILE EXAMINATION GLOVES WITH LANO-E AND PEPPERMINT CITRUS SCENT.

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