Medical Device Manufacturer · US , Frederick , MD

Dr. Howard Martin, P.A. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dr. Howard Martin, P.A. Dental ✕

3 devices

1-3 of 3

Cleared Jun 26, 2006

TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)

Cleared Jul 27, 1998

MCS-MEDICATED CANAL SEALER

Cleared Jul 21, 1997

ANTIBACTERIAL GUTTA PERCHA

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026