Lyme-ID IgG Test; Bio-ID800
Nov 2025
86d
Inanovate, Inc.
1
Total
1
Cleared
0
Denied
Inanovate, Inc. — FDA 510(k) Submissions
Inanovate, Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Reagent, Borrelia Serological Reagent . Use the specialty filter in the sidebar to narrow results.
1 devices