Hindernis DE Mexico, S.A.P.I. DE C.V. is one of 9 FDA 510(k) medical device manufacturers from Mexico in the dataset, ranked by real submission volume.
Hindernis DE Mexico, S.A.P.I. DE C.V. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hindernis DE Mexico, S.A.P.I. DE C.V. has 1 FDA 510(k) cleared medical devices. Based in Naucalpan De Juarez, MX.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hindernis DE Mexico, S.A.P.I. DE C.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Manton Business and Technology Services as regulatory consultant.
Hindernis DE Mexico, S.A.P.I. DE C.V. — FDA 510(k) Products and Clearance History
1 devices