Medical Device Manufacturer · US , Portsmouth , NH

Dr. Bernard Loewenthal - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987
1
Total
1
Cleared
0
Denied

Dr. Bernard Loewenthal has 1 FDA 510(k) cleared medical devices. Based in Portsmouth, US.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dr. Bernard Loewenthal Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dr. Bernard Loewenthal

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