510(k) Report

FDA applicant

National Center For Pelvic Pain Research Devices,

Sebastopol, CA1 decision2012–20120 recalls

FDA records 1 decision for National Center For Pelvic Pain Research Devices, (Sebastopol, CA) in 2012: 1 De Novo grant. All are in product code OSD (Massager, Therapeutic, To Internally Massage…). 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, physical medicine panel, where it files most

How often FDA has decided National Center For Pelvic Pain Research Devices,’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — National Center For Pelvic Pain Research Devices, by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like National Center For Pelvic Pain…’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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Which product codes does it file in?

  • OSDMassager, Therapeutic, To Internally Massage Trigger Points In The Pelvic Floor…1decision

What has FDA decided for it lately?

  • DEN100023Ahip Internal Trigger Point Wand Model: 1National Center For Pelvic Pain Research Devices, · 2012

The one decision as National Center For Pelvic Pain Research Devices, →