510(k) Report

FDA applicant

Mumease

Charlotte, NC1 decision2020–20200 recalls

FDA records 1 decision for Mumease (Charlotte, NC) in 2020: 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 Mumease’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Mumease by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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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 2 times; 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.

  • K193374TumEase Acupressure BraceletsMumease · 20202cite it

What has FDA decided for it lately?

  • K193374TumEase Acupressure BraceletsMumease · 2020

The one decision as Mumease →