FDA applicant

Horizon Medical, Inc.

Santa Ana, CA3 decisions1988–19980 recalls

FDA records 3 decisions for Horizon Medical, Inc. (Santa Ana, CA) from 1988 to 1998: 3 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and KMJ (Lubricant, Patient). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Horizon Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Horizon”

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

Horizon Medical Products, Inc. 16 Horizon Diagnostics, Inc. 7 Horizon Chemical Co. 1 Horizon Surgical, Inc. 1

Horizon Medical, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Horizon”