FDA applicant

Apollo Enterprise, Ltd. Co.

Somerset, WI3 decisions1988–19910 recalls

FDA records 3 decisions for Apollo Enterprise, Ltd. Co. (Somerset, WI) from 1988 to 1991: 3 510(k) clearances. Most are in product codes FRW (Scale, Patient) and HIS (Condom). 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 Apollo Enterprise, Ltd. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Apollo Enterprise, Ltd. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Apollo”

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

Apollo Endosurgery, Inc. 14 Apollo Spine, Inc. 7 Apollo Medical Imaging Technology Pty., Ltd. 2 Apollo Dental Products, Inc. 2 Apollo Products, Inc. 1 Apollo'S Suntanning Supplies 1 Apollo Medical Optics, Ltd. 1 Apollo Fluid Dynamics 1 Apollo Corp. 1 Apollo Physical Therapy Products International 1

Apollo Enterprise, Ltd. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Apollo”