FDA applicant

Kerr Corporation (Danbury)

Washington, DC32 decisions1978–20051 recall

FDA records 32 decisions for Kerr Corporation (Danbury) (Washington, DC) from 1978 to 2005: 32 510(k) clearances. Most are in product codes KLE (Agent, Tooth Bonding, Resin) and EMA (Cement, Dental). 1 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 Kerr Corporation (Danbury)’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kerr Corporation (Danbury) since 2007.

Recalls per year

1in 2014

2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Kerr Corporation (Danbury) by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Kerr”

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

Kerr Corporation 41 Kerr Dental Materials Center 17 Kerr Hearing Aid Laboratory 1

Kerr Corporation (Danbury)

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Kerr”