510(k) Report

FDA applicant

Bebig, Inc.

New York, NY1 decision1994–19940 recalls

FDA records 1 decision for Bebig, Inc. (New York, NY) in 1994: 1 510(k) clearance. 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 Bebig, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bebig, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bebig, Inc. 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, Radionuclide1decision

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.

  • K931393Bebig Plaques RUM101-RUM114Bebig, Inc. · 19941cites it

What has FDA decided for it lately?

  • K931393Bebig Plaques RUM101-RUM114Bebig, Inc. · 1994

The one decision as Bebig, Inc. →

Other applicant names beginning “Bebig”

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

Bebig Isotopen-Und Medizintechnik GmbH 3Bebig Isotopentechnik GmbH 1Bebig Trade, Inc. 1