510(k) Report

FDA applicant

Sharps Terminator, LLC

Lubbock1 decision2016–20160 recalls

FDA records 1 decision for Sharps Terminator, LLC (Lubbock) in 2016: 1 original PMA approval. All are in product code MTV (Sharps Needle Destruction Device). 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, general hospital panel, where it files most

How often FDA has decided Sharps Terminator, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Sharps Terminator, LLC by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sharps Terminator, LLC’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?

  • MTVSharps Needle Destruction Device1decision

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.

  • P120018Sharps TerminatorSharps Terminator, LLC · 20161cites it

What has FDA decided for it lately?

  • P120018Sharps TerminatorSharps Terminator, LLC · 2016

The one decision as Sharps Terminator, LLC →

Other applicant names beginning “Sharps”

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

Sharps Compliance, Inc. 2