510(k) Report

FDA applicant

Ryan Telemedicine

Costa Mesa, CA2 decisions2003–20030 recalls

FDA records 2 decisions for Ryan Telemedicine (Costa Mesa, CA) in 2003: 2 510(k) clearances. All are in product code IPF (Stimulator, Muscle, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Ryan Telemedicine’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ryan Telemedicine since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ryan Telemedicine’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?

  • IPFStimulator, Muscle, Powered2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K030254Interferential Stimulator, Model RTM1000Ryan Telemedicine · 20031cites it

What has FDA decided for it lately?

  • K031884Interferential Stimulator, Model NetwaveRyan Telemedicine · 2003
  • K030254Interferential Stimulator, Model RTM1000Ryan Telemedicine · 2003

All 2 as Ryan Telemedicine →

Other applicant names beginning “Ryan”

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

Ryan Medical, Inc. 5