Gri-Alleset, Inc.

Gri-Alleset, Inc. — FDA 510(k) Submissions

Gri-Alleset, Inc. has submitted 4 FDA 510(k) premarket notifications since 2021, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature, Gown, Isolation, Surgical, Mask, Surgical . Use the specialty filter in the sidebar to narrow results.