FDA applicant

Genesis Industries, Inc.

Mchenry, IL17 decisions1983–20000 recalls

FDA records 17 decisions for Genesis Industries, Inc. (Mchenry, IL) from 1983 to 2000: 17 510(k) clearances. Most are in product codes EIS (Remover, Crown) and GAA (Needle, Aspiration And Injection, Disposable). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Genesis Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Genesis Industries, 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 “Genesis”

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

Genesis Fracture Care, Inc. 5 Genesis Biosystems, Inc. 4 Genesis Labs, Inc. 3 Genesis Orthopedics, Inc. 2 Genesis Digital Imaging, Inc. 2 Genesis Software Innovations 2 Genesis Medical, Inc. 2 Genesis Medical Interventional, Inc. 2 Genesis Medical Technology, Inc. 1 Genesis Health Technologies 1 Genesis Air, Inc. 1 Genesis Health Light Corporation 1

Genesis Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Genesis”