FDA applicant
Xtal Corp.
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
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.
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.
See the 510(k) Report