FDA applicant

Kerr Dental Materials Center

Orange, CA17 decisions1996–20051 recall

FDA records 17 decisions for Kerr Dental Materials Center (Orange, CA) from 1996 to 2005: 17 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and KLE (Agent, Tooth Bonding, Resin). 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 Dental Materials Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kerr Dental Materials Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kerr Dental Materials Center by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kerr Dental Materials Center’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 Corporation (Danbury) 32 Kerr Hearing Aid Laboratory 1

Kerr Dental Materials Center

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”