FDA applicant

Medart Corp.

San Diego, CA5 decisions1999–20010 recalls

FDA records 5 decisions for Medart Corp. (San Diego, CA) from 1999 to 2001: 5 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). 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 Medart Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medart Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Medart”

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

Medart A/S 3

Medart Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medart”