FDA applicant

Pain Management Technologies

Akron, OH6 decisions2001–20220 recalls

FDA records 6 decisions for Pain Management Technologies (Akron, OH) from 2001 to 2022: 6 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and GXY (Electrode, Cutaneous). Its devices cite 9 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Pain Management Technologies, Inc.”.

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 Management Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pain Management Technologies’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 Relief Technologies 3 Pain Prevention Laboratory, Inc. 1 Pain Prevention, Inc. 1 Pain Concepts, Inc. 1

Pain Management Technologies

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Pain”