FDA Device Intelligence
Home › LUNEAU TECHNOLOGY OPERATIONS › VISIONIX

VISIONIX

LUNEAU TECHNOLOGY OPERATIONS · Model VX220 · UDI-DI 03664188002200

HKXMXK Prescription
10
510(k) clearances
4
Adverse events
0
Recalls
38
Facilities

Description

The VX220 is a multifunctional eye diagnostic device. There are several operation modes combined in a single platform: keratometer, corneal topographer, tonometer,and pachymeter and retro illumination

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.