510(k) Report

FDA applicant

Kramer Const

Palo Alto, CA1 decision1991–19910 recalls

FDA records 1 decision for Kramer Const (Palo Alto, CA) in 1991: 1 510(k) clearance. All are in product code LRY (Punch, Surgical). 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 Kramer Const’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kramer Const since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kramer Const 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?

  • LRYPunch, Surgical1decision

What has FDA decided for it lately?

  • K904869Ellipse PunchKramer Const · 1991

The one decision as Kramer Const →