510(k) Report

FDA applicant

Dr. Howard Martin, P.A.

Frederick, MD3 decisions1997–20060 recalls

FDA records 3 decisions for Dr. Howard Martin, P.A. (Frederick, MD) from 1997 to 2006: 3 510(k) clearances. Most are in product codes EKM (Gutta-Percha) and EMA (Cement, Dental). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Dr. Howard Martin, P.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. Howard Martin, P.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. Howard Martin, P.A. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EKMGutta-Percha2decisions
  • EMACement, Dental1decision

What has FDA decided for it lately?

  • K051573TGP (Gutta Percha Containing Tetracycline or Doxycycline)Dr. Howard Martin, P.A. · 2006
  • K973636MCS-Medicated Canal SealerDr. Howard Martin, P.A. · 1998
  • K971641Antibacterial Gutta PerchaDr. Howard Martin, P.A. · 1997

All 3 as Dr. Howard Martin, P.A. →