FDA applicant

Cleveland Tubing, Inc.

Cleveland, TN4 decisions1993–19940 recalls

FDA records 4 decisions for Cleveland Tubing, Inc. (Cleveland, TN) from 1993 to 1994: 4 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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, anesthesiology panel, where it files most

How often FDA has decided Cleveland Tubing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cleveland Tubing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cleveland Tubing, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cleveland Tubing, Inc.’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 “Cleveland”

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

Cleveland Medical Devices, Inc. 8 Cleveland Diagnostics, Inc. 1 Cleveland Medical Supply & Services 1 Cleveland Clinic 1 Cleveland Clinic Foundation 1

Cleveland Tubing, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cleveland”