FDA applicant

Aesthetech Corp.

Paso Robles, CA6 decisions1981–19870 recalls

FDA records 6 decisions for Aesthetech Corp. (Paso Robles, CA) from 1981 to 1987: 6 510(k) clearances. Most are in product codes LZK (Implant, Malar) and LCJ (Tissue Expander And Accessories). 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 Aesthetech Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aesthetech Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aesthetech Corp.

Which product codes does it file in?

What has FDA decided for it lately?