Argos Infinity (Rev. 1.0)
Feb 2026
143d
Retia Medical Systems, Inc.
1
Total
1
Cleared
0
Denied
Retia Medical Systems, Inc. — FDA 510(k) Submissions
Retia Medical Systems, Inc. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Computer, Diagnostic, Pre-programmed, Single-function . Use the specialty filter in the sidebar to narrow results.
1 devices