510(k) Report

FDA applicant

Woodside Biomedical, Inc.

San Diego, CA6 decisions1998–20020 recalls

FDA records 6 decisions for Woodside Biomedical, Inc. (San Diego, CA) from 1998 to 2002: 6 510(k) clearances. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Its devices cite 6 predicates, 5 of them its own earlier devices. 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, neurology panel, where it files most

How often FDA has decided Woodside Biomedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Woodside Biomedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Woodside Biomedical, 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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Which product codes does it file in?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief6decisions

Whose devices does it build on?

Its devices cite 6 predicates; 5 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 13 times; 5 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.

  • K020180Reliefband Device, Models RB-DL, RB-EL, RB-RLWoodside Biomedical, Inc. · 20023cite it
  • K980333ReliefbandWoodside Biomedical, Inc. · 19982cite it
  • K982967Reliefband MST Device, Models RB-2, RB-6, RB-RWoodside Biomedical, Inc. · 19992cite it
  • K994387Reliefband NST Device, Model WB-2L, WB-6L, WB-RLWoodside Biomedical, Inc. · 20002cite it
  • K983907Reliefband NST Device Models WB-2,WB-6,WB-RWoodside Biomedical, Inc. · 19992cite it
  • K982436Reliefband NST Device, Model #'S WB-2, WB-6 and WB-RWoodside Biomedical, Inc. · 19982cite it

What has FDA decided for it lately?

  • K020180Reliefband Device, Models RB-DL, RB-EL, RB-RLWoodside Biomedical, Inc. · 2002
  • K994387Reliefband NST Device, Model WB-2L, WB-6L, WB-RLWoodside Biomedical, Inc. · 2000
  • K983907Reliefband NST Device Models WB-2,WB-6,WB-RWoodside Biomedical, Inc. · 1999
  • K982967Reliefband MST Device, Models RB-2, RB-6, RB-RWoodside Biomedical, Inc. · 1999
  • K982436Reliefband NST Device, Model #'S WB-2, WB-6 and WB-RWoodside Biomedical, Inc. · 1998
  • K980333ReliefbandWoodside Biomedical, Inc. · 1998

All 6 as Woodside Biomedical, Inc. →