510(k) Report

FDA applicant

Pressure Point, Inc.

Tinton Falls, NJ1 decision2014–20140 recalls

FDA records 1 decision for Pressure Point, Inc. (Tinton Falls, NJ) in 2014: 1 510(k) clearance. All are in product code MVV (Device, Acupressure). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

1in 2014

2014: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Pressure Point, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Which product codes does it file in?

  • MVVDevice, Acupressure1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K142471Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist StripPressure Point, Inc. · 20141cites it

What has FDA decided for it lately?

  • K142471Pressure Right, Single-Use, Disposable, Acupressure, Pressure-Sensitive Wrist StripPressure Point, Inc. · 2014

The one decision as Pressure Point, Inc. →

Other applicant names beginning “Pressure”

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

Pressure Products Medical Device Manufacturing, LLC 9Pressure-Tech, Inc. 1Pressure Products, Inc. 1