510(k) Report

FDA applicant

Baron Technologies, Inc.

Salt Lake City, UT2 decisions1986–19870 recalls

FDA records 2 decisions for Baron Technologies, Inc. (Salt Lake City, UT) from 1986 to 1987: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FOZ (Catheter, Intravascular, Therapeutic…). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Baron Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Baron Technologies, 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?

  • FMFSyringe, Piston1decision
  • FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1decision

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.

  • K862480BT Cath (Intravascular Catheter)Baron Technologies, Inc. · 19861cites it

What has FDA decided for it lately?

  • K864541BT Hypodermic SyringeBaron Technologies, Inc. · 1987
  • K862480BT Cath (Intravascular Catheter)Baron Technologies, Inc. · 1986

All 2 as Baron Technologies, Inc. →

Other applicant names beginning “Baron”

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

Baron Trading, Inc. 1