510(k) Report

FDA applicant

Arnold Technologies

Leesburg, FL2 decisions1987–19870 recalls

FDA records 2 decisions for Arnold Technologies (Leesburg, FL) in 1987: 2 510(k) clearances. All are in product code EXB (Collector, Ostomy). 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 Arnold Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arnold Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • EXBCollector, Ostomy2decisions

What has FDA decided for it lately?

  • K872294Combination Nite Drainage UnitArnold Technologies · 1987
  • K870136Personal PunchArnold Technologies · 1987

All 2 as Arnold Technologies →

Other applicant names beginning “Arnold”

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

Arnold & Richter Cine Technik 2Arnold & Sons 1Arnold & Porter For G.E. Co. 1Arnold Tuber Industries 1