Grindguard, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Grindguard, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Feb 2026. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Grindguard, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.
2 devices