Not currently registered with FDA under this name

Dr. Howard Martin, P.A.

Frederick, MD, United States. Named as applicant on 3 dental 510(k) clearances between 1997 and 2006. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 31997–2006
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Dr. Howard Martin, P.A. as the applicant.

Decided	510(k)	Device	Device type
26 Jun 2006	K051573	TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)	EKM Gutta-Percha
27 Jul 1998	K973636	MCS-MEDICATED CANAL SEALER	EMA Dental Cement
21 Jul 1997	K971641	ANTIBACTERIAL GUTTA PERCHA	EKM Gutta-Percha

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.