Facet Technologies, LLC

Facet Technologies, LLC — FDA 510(k) Submissions

Facet Technologies, LLC has submitted 7 FDA 510(k) premarket notifications since 2014, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Multiple Use Blood Lancet For Single Patient Use Only, Needle, Hypodermic, Single Lumen, Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature, Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature . Use the specialty filter in the sidebar to narrow results.