Aladdin-M

FDA UDI

Class II (US FDA UDI)

by Visia Imaging Srl

Identity

Trade Name: ALADDIN-M FDA UDI
Generic Name: Corneal topography system analyser FDA UDI
Model / Reference: 1240213 FDA UDI

Identifiers

Primary DI / UDI-DI: 08034028770364 FDA UDI
510(k) Number: K160327 FDA UDI
FDA Product Code: HJO FDA UDI
GMDN Term: Corneal topography system analyser FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.1850 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Corneal topography system analyser

Aladdin-M by Visia Imaging Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal topography system analyser.

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MOPTIM — Shenzhen CERTAINN Technology Co., Ltd. · Class I
Corneal Topographer — CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO., LTD · Class I
WAVE ANALYZER MEDICA 700 PLUS — ESSILOR INTERNATIONAL · Class II
TearCheck T — E-Swin · Class I
ALADDIN TMS — VISIA IMAGING SRL · Class II

Cleared under the same submission

K160327 also covers:

ALADDIN HW3.0 — VISIA IMAGING SRL
SeeNA — VISIA IMAGING SRL

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Visia Imaging Srl

Sources (1)

FDA UDI a81d9bdf-7013-475c-b505-855a7445328e 33 fields · synced May 30, 2026