510(k) Report

FDA applicant

The Gid Group, Inc.

Boulder, CO1 decision2012–20121 recall

FDA records 1 decision for The Gid Group, Inc. (Boulder, CO) in 2012: 1 510(k) clearance. All are in product code MUU (System, Suction, Lipoplasty). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 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, general and plastic surgery panel, where it files most

How often FDA has decided The Gid Group, Inc.’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

1in 2017

2017: 1
2012high 1 (2017) · low 0 (2012)2026

Class I Class II/III not classified

FIG. 1 — The Gid Group, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Gid Group, Inc.’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?

  • MUUSystem, Suction, Lipoplasty1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 5 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.

  • K120902GID 700The Gid Group, Inc. · 20125cite it

What has FDA decided for it lately?

  • K120902GID 700The Gid Group, Inc. · 20121 recall

The one decision as The Gid Group, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K120902REVOLVE ADVANCED ADIPOSE SYSTEM, for aspiration, harvesting, filtering, and transferring…Aug 8, 2017Class II