FDA applicant

Virtual Incision

Lincoln, NE2 decisions2024–20260 recalls

FDA records 2 decisions for Virtual Incision (Lincoln, NE) from 2024 to 2026: 1 510(k) clearance and 1 De Novo grant. All are in product code SAB (Table Mounted Miniaturized Electromechanical…). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Virtual Incision’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Virtual Incision by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Virtual Incision’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 “Virtual”

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

Virtual Imaging, Inc. 9 Virtual Corp. 9 Virtual Radiologic Corporation 3 Virtual Ports, Ltd. 2

Virtual Incision

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Virtual”