FDA applicant

Pain Relief Technologies

Beaverton, OR3 decisions2006–20120 recalls

FDA records 3 decisions for Pain Relief Technologies (Beaverton, OR) from 2006 to 2012: 3 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and NUH (Stimulator, Nerve, Transcutaneous…). 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, neurology panel, where it files most

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

FDA decisions per year

1in 2012

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pain”

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

Pain Management Technologies 6 Pain Prevention Laboratory, Inc. 1 Pain Prevention, Inc. 1 Pain Concepts, Inc. 1

Pain Relief Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pain”