FDA applicant

Compression Works, LLC

Providence, RI3 decisions2011–20230 recalls

FDA records 3 decisions for Compression Works, LLC (Providence, RI) from 2011 to 2023: 3 510(k) clearances. All are in product code DXC (Clamp, Vascular). Its devices cite 6 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Compression Works, Inc.”.

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

FIG. A — Illustration, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2023

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Compression Works, LLC by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Compression Works, 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

Other applicant names beginning “Compression”

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

Compression Therapy Concepts, Inc. 8 Compression Splint Products, Inc. 1 Compression Technologies Unlimited, Inc. 1

Compression Works, LLC

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Compression”