RecallHawk

Cube 4D Navigation System, VirtuEye Pro

Fiagon GmbH

Summary

Fiagon GmbH received 510(k) clearance for Cube 4D Navigation System, VirtuEye Pro, a PGW device. Cleared on 2026-06-02.

Details

Source

510(k) Clearance

External ID

K261540

Action Date

2026-06-02

Status

Special

Category

device

Product Code

PGW

Product Description

Cube 4D Navigation System, VirtuEye Pro. Product code: PGW.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Fiagon GmbH has received 4 total clearances in our database.

Fiagon GmbH has 4 FDA actions in our database, including 4 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Fiagon GmbH have FDA actions?

Fiagon GmbH has 4 FDA actions in our database, including 0 recalls and 4 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K261540" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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