510(k) Report

FDA applicant

Sourcetech Medical, LLC

Carol Stream, IL3 decisions1999–20030 recalls

FDA records 3 decisions for Sourcetech Medical, LLC (Carol Stream, IL) from 1999 to 2003: 3 510(k) clearances. All are in product code KXK (Source, Brachytherapy, Radionuclide). 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, radiology panel, where it files most

How often FDA has decided Sourcetech Medical, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sourcetech Medical, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KXKSource, Brachytherapy, Radionuclide3decisions

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.

  • K023210Seedlinks, Models 70301, 70302, 70303Sourcetech Medical, LLC · 20031cites it

What has FDA decided for it lately?

  • K023210Seedlinks, Models 70301, 70302, 70303Sourcetech Medical, LLC · 2003
  • K991881125-Implant Seeds, Model STM1250Sourcetech Medical, LLC · 2000
  • K991280125 Implant Seeds, Model STM1251Sourcetech Medical, LLC · 1999

All 3 as Sourcetech Medical, LLC →