FDA applicant

Arent, Fox, Kintner, Plotkin & Kahn

Washington, DC1 decision1997–19970 recalls

FDA records 1 decision for Arent, Fox, Kintner, Plotkin & Kahn (Washington, DC) in 1997: 1 510(k) clearance. All are in product code 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 Arent, Fox, Kintner, Plotkin & Kahn’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arent, Fox, Kintner, Plotkin & Kahn since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arent, Fox, Kintner, Plotkin & Kahn by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Arent”

FDA records each applicant name separately; these may or may not be the same firm.

Arent Fox 4

Arent, Fox, Kintner, Plotkin & Kahn

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arent”