510(k) Report

FDA applicant

Pinyons Medical Technology, Inc.

Park City, UT3 decisions2007–20070 recalls

FDA records 3 decisions for Pinyons Medical Technology, Inc. (Park City, UT) in 2007: 3 510(k) clearances. All are in product code FMF (Syringe, Piston). 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 Pinyons Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2007

2007: 3
2007high 3 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pinyons Medical Technology, 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, Piston3decisions

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.

  • K072299Powrsyringe AspiratorPinyons Medical Technology, Inc. · 20071cites it

What has FDA decided for it lately?

  • K072299Powrsyringe AspiratorPinyons Medical Technology, Inc. · 2007
  • K072345Powrsyringe MonitorPinyons Medical Technology, Inc. · 2007
  • K072318Powrsyringe InjectorPinyons Medical Technology, Inc. · 2007

All 3 as Pinyons Medical Technology, Inc. →