FDA applicant

Xanar, Inc.

Colorado Springs, CO12 decisions1983–19860 recalls

FDA records 12 decisions for Xanar, Inc. (Colorado Springs, CO) from 1983 to 1986: 12 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and LNK (Laser For Gastro-Urology Use). 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 Xanar, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Xanar, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Xanar, Inc.’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

Xanar, Inc.

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?