510(k) Report

FDA applicant

Atlas Surgical Belt Co., Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Atlas Surgical Belt Co., Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code EXB (Collector, Ostomy). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Atlas Surgical Belt Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Atlas Surgical Belt Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Atlas Surgical Belt Co., 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

Which product codes does it file in?

  • EXBCollector, Ostomy1decision

What has FDA decided for it lately?

  • K842119Ostomy or Urostomy Abdominal Belt OSAtlas Surgical Belt Co., Inc. · 1984

The one decision as Atlas Surgical Belt Co., Inc. →

Other applicant names beginning “Atlas”

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

Atlas Spine, Inc. 19Atlas Researches, Ltd. 4Atlas Medical 2Atlas Medical Products, Inc. 1Atlas Technology 1Atlas Link Technology Co., Ltd. 1