JFord Speculum Sleeve?
Mar 2026
234d
Ford Medtech, LLC
1
Total
1
Cleared
0
Denied
Ford Medtech, LLC — FDA 510(k) Submissions
Ford Medtech, LLC 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 Speculum, Vaginal, Nonmetal . Use the specialty filter in the sidebar to narrow results.
1 devices