510(k) Report

FDA applicant

American Safety Razor Co.

Staunton, VA4 decisions1977–19930 recalls

FDA records 4 decisions for American Safety Razor Co. (Staunton, VA) from 1977 to 1993: 4 510(k) clearances. Most are in product codes GES (Blade, Scalpel) and MDM (Instrument, Manual, Surgical, General Use). 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 American Safety Razor Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Safety Razor Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like American Safety Razor Co.’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

Which product codes does it file in?

  • GESBlade, Scalpel2decisions
  • MDMInstrument, Manual, Surgical, General Use1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K924503Personna Safety ScalpelAmerican Safety Razor Co. · 19931cites it

What has FDA decided for it lately?

  • K924503Personna Safety ScalpelAmerican Safety Razor Co. · 1993
  • K873142Personna Disposable ScalpelAmerican Safety Razor Co. · 1987
  • K863557Blade, Surgical Preparation Razor, Straight,SingleAmerican Safety Razor Co. · 1986
  • K771045Blades, ScalpelAmerican Safety Razor Co. · 1977

All 4 as American Safety Razor Co. →