510(k) Report

FDA applicant

Teledyne Densco

Mchenry, IL4 decisions1978–19820 recalls

FDA records 4 decisions for Teledyne Densco (Mchenry, IL) from 1978 to 1982: 4 510(k) clearances. Most are in product codes EHK (Cup, Prophylaxis) and EJL (Bur, 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 Teledyne Densco’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teledyne Densco since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Teledyne”

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