FDA applicant

Xanmed Corp.

Washington, DC9 decisions1984–19870 recalls

FDA records 9 decisions for Xanmed Corp. (Washington, DC) from 1984 to 1987: 9 510(k) clearances. Most are in product codes DYB (Introducer, Catheter) and LXH (Orthopedic Manual 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, cardiovascular panel, where it files most

How often FDA has decided Xanmed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Xanmed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Xanmed Corp.’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

Xanmed Corp.

Which product codes does it file in?

What has FDA decided for it lately?