FDA applicant

Well Being Ent.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Well Being Ent. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code KDH (Catheter (Gastric, Colonic, Etc.), Irrigation…). 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 Well Being Ent.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Well Being Ent. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Well”

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

Well-Life Healthcare Limited 29 Well Lead Medical Co., Ltd. 17 Well Lead Medical Instruments 4 Well Brain International, Ltd. 4 Well Success Biotech, Inc. 3 Well Lead Medical (Hainan) Co., Ltd. 1 Well-Life Consultant 1 Well Arts Optical Factory, Ltd. 1 Well Lead Instruments 1 Well Care (Wuhan) Medical Technology Co., Ltd. 1 Well Home Health Products Co. 1

Well Being Ent.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Well”