510(k) Report

FDA applicant

Dental Power, Inc.

Dana Point, CA2 decisions1994–20010 recalls

FDA records 2 decisions for Dental Power, Inc. (Dana Point, CA) from 1994 to 2001: 2 510(k) clearances. Most are in product codes EKS (File, Pulp Canal, Endodontic) and ELR (Post, Root Canal). 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 Dental Power, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Power, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dental Power, Inc.’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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