# K131567: Aladdin

- Pathway: 510(k) (Traditional)
- Applicant: Visia Imaging S.R.L.
- Decided: Jun 5, 2014 after 371 days
- Product code: HJO (Biomicroscope, Slit-Lamp, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
ALADDIN is intended for biometric determination of the following ocular measures: axial length, corneal radius, conical cylinder axis, anterior chamber depth, white-to-white (WTW) and pupil diameter of the human eye. ALADDIN also measures corneal topography. For patients who are candidates for intraocular lens (JOL) implantation, ALADDIN also aids in the calculation of the appropriate IOL power and type to be implanted. ALADDIN is intended for use by physicians and eye-care professionals and may only be used under the supervision of a physician.

Source page: https://510kreport.com/device/K131567
Methodology: https://510kreport.com/methodology