510(k) Report

FDA applicant

Medical Compression Systems (Dbn), Ltd.

Ra'Ananna 43373, IL10 decisions2000–20162 recalls

FDA records 10 decisions for Medical Compression Systems (Dbn), Ltd. (Ra'Ananna 43373, IL) from 2000 to 2016: 10 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and IRP (Massager, Powered Inflatable Tube). Its devices cite 17 predicates, 9 of them its own earlier devices. 2 recalls are linked to its devices.

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 Medical Compression Systems (Dbn), Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2011: 12012: 12014: 12016: 1
2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

2in 2011

2011: 2
2007high 2 (2011) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Medical Compression Systems (Dbn), Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medical Compression Systems (Dbn), Ltd.’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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