510(k) Report

FDA applicant

Xtal Corp.

Solana Beach, CA3 decisions1985–19860 recalls

FDA records 3 decisions for Xtal Corp. (Solana Beach, CA) from 1985 to 1986: 3 510(k) clearances. Most are in product codes HRM (Microscope, Operating & Accessories…) and HNN (Knife, Ophthalmic). 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 Xtal Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Xtal Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Xtal Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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