510(k) Report

FDA applicant

Digital Doc, LLC

Los Angeles, CA1 decision1998–19980 recalls

FDA records 1 decision for Digital Doc, LLC (Los Angeles, CA) in 1998: 1 510(k) clearance. All are in product code EIA (Unit, Operative 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 Digital Doc, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Digital Doc, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • EIAUnit, Operative Dental1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K981663Digital DocDigital Doc, LLC · 19982cite it

What has FDA decided for it lately?

  • K981663Digital DocDigital Doc, LLC · 1998

The one decision as Digital Doc, LLC →