510(k) Report

FDA applicant

Beampoint AB

Minneapolis,, MN1 decision2005–20050 recalls

FDA records 1 decision for Beampoint AB (Minneapolis,, MN) in 2005: 1 510(k) clearance. All are in product code EZL (Catheter, Retention Type, Balloon). Its devices cite 4 predicates, 0 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Beampoint AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Beampoint AB’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?

  • EZLCatheter, Retention Type, Balloon1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 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.

  • K042110BeamcathBeampoint AB · 20053cite it

What has FDA decided for it lately?

  • K042110BeamcathBeampoint AB · 2005

The one decision as Beampoint AB →