FDA applicant

Selomas, Inc.

Mchenry, IL7 decisions1981–19860 recalls

FDA records 7 decisions for Selomas, Inc. (Mchenry, IL) from 1981 to 1986: 7 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and FQL (Stocking, Medical Support (For General Medical…). 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 Selomas, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Selomas, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Selomas, 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

Selomas, Inc.

Which product codes does it file in?

What has FDA decided for it lately?