FDA applicant

Ximed Medical Systems

Santa Clara, CA11 decisions1989–19960 recalls

FDA records 11 decisions for Ximed Medical Systems (Santa Clara, CA) from 1989 to 1996: 11 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and 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 Ximed Medical Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ximed Medical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Ximed”

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

Ximed/Prosure/Injectx 9

Ximed Medical Systems

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 “Ximed”