510(k) Report

FDA applicant

Lode Corp.

Seattle, WA3 decisions1985–20200 recalls

FDA records 3 decisions for Lode Corp. (Seattle, WA) from 1985 to 2020: 3 510(k) clearances. Most are in product codes ISD (Exerciser, Measuring) and JPA (System, Multipurpose For In Vitro Coagulation…). No recall is linked to its devices.

FDA’s records also spell it “Lode B.V.”.

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 Lode Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lode Corp.’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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Which product codes does it file in?

  • ISDExerciser, Measuring2decisions
  • JPASystem, Multipurpose For In Vitro Coagulation Studies1decision

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.

  • K851097Lode Model Corival ErgometerLode Corp. · 19852cite it

What has FDA decided for it lately?

  • K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR…Lode B.V. · 2020
  • K852450Lode Coagulometer Model LC-6Lode Corp. · 1985
  • K851097Lode Model Corival ErgometerLode Corp. · 1985

All 2 as Lode Corp. →The one decision as Lode B.V. →