510(k) Report

FDA applicant

Rahn Laboratories

Bland, VA3 decisions1988–19900 recalls

FDA records 3 decisions for Rahn Laboratories (Bland, VA) from 1988 to 1990: 3 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and LYY (Latex Patient Examination Glove). 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 Rahn Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rahn Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rahn Laboratories 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?

  • KKXDrape, Surgical, Antimicrobial1decision
  • LYYLatex Patient Examination Glove1decision
  • GESBlade, Scalpel1decision

What has FDA decided for it lately?

  • K900266Sterile Carbon Steel Surgical BladeRahn Laboratories · 1990
  • K892461Non-Sterile Latex Examination GlovesRahn Laboratories · 1989
  • K881479Operation Room TowelRahn Laboratories · 1988

All 3 as Rahn Laboratories →