510(k) Report

FDA applicant

Nova/Da Vinci Systems, Inc.

San Diego, CA1 decision2000–20000 recalls

FDA records 1 decision for Nova/Da Vinci Systems, Inc. (San Diego, CA) in 2000: 1 510(k) clearance. All are in product code EBZ (Activator, Ultraviolet, For Polymerization). 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, dental panel, where it files most

How often FDA has decided Nova/Da Vinci Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nova/Da Vinci Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nova/Da Vinci Systems, Inc.’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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Other applicant names beginning “Nova/Da”

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