510(k) · Cleared

Cleared

Laser Indirect Ophthalmoscope 500(Lio-500)

K113390510(k) TraditionalCleared Feb 14, 201290-day reviewClass II21 CFR 878.4810

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Meridian AG · GEX Powered Laser Surgical Instrument

Cleared on Feb 14, 2012 as substantially equivalent to K013402 (Carl Zeiss, Inc., 2001) after a 90-day review. Its family tree reaches back 2 generations to 1993.

Decided: Feb 14, 2012
Review: 90 days
Class: Class II
Product code: GEX
Recalls: None
Predicates: 1

Its longest line of descent runs back 2 generations to K925642 (1993). No later device cites it as a predicate yet.

By dateBy generation

Root · 2 generations backK925642 Zeiss Diode-Pumped Solid State LaserCarl Zeiss, Inc. · 1993
1 generation backK013402 Visulas 532SCarl Zeiss, Inc. · 2001 · Recalled
This deviceK113390 Laser Indirect Ophthalmoscope 500(Lio-500)Meridian AG · 2012

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K925642	Zeiss Diode-Pumped Solid State Laser	Carl Zeiss, Inc.	1993	—
−1	K013402	Visulas 532S	Carl Zeiss, Inc.	2001	1
0 (this device)	K113390	Laser Indirect Ophthalmoscope 500(Lio-500)	Meridian AG	2012	—

FIG. 1 — Lineage of K113390, 1993–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GEX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new GEX device

#1 K222064 The Alma Soprano Titaniumscore 38.1 · 24 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K013402	Visulas 532S Summary page 1 …halmic Surgical Laser Classification Name: Powered Laser Surgical Instrument Predicate Device: VISULAS 532S manufactured by CARL ZEISS, INC. and cleared under 510(k) # K013402 Device Description: The LIO-500 can be used on a 532 nmn laser such as the MERILAS 532a or any other ophthalmic laser with 532…	Carl Zeiss, Inc.	2001	1

Also cleared against K013402: 4 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

The line of descent spans 19 years and passes through 2 companies; a new generation was cleared every 10.3 years on median.
1 of the 2 ancestors has a recall of any class.
4 other devices also cite its predicate K013402.

How does its category compare?

All GEX devices

GEX Powered Laser Surgical Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · GEX

83in 2025

2007high 107 (2008) · low 41 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEX

90in 2025

2007high 152 (2022) · low 78 (2018)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GEX

3in 2024

2007high 18 (2011) · low 0 (2009)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GEX

2,720in 2025

2007high 3,525 (2018) · low 209 (2009)2025

MAUDE reports naming product code GEX, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	73	79	9	342
2008	107	86	2	232
2009	69	100	0	209
2010	50	96	4	1,711
2011	41	83	18	3,024
2012	45	118	5	2,000
2013	46	144	3	2,236
2014	61	147	6	2,036
2015	47	112	0	2,099
2016	51	114	1	2,585
2017	67	90	5 (1)	2,977
2018	51	78	5	3,525
2019	41	88	6	2,709
2020	52	90	1	2,183
2021	53	123	0	3,465
2022	60	152	0	2,288
2023	52	87	6	2,337
2024	82	90	3	2,187
2025	83	90	0	2,720
2026	57	90	2	—

What is it indicated for?

The Laser Indirect Ophthalmoscope 500 (LIO-500) is intended for use in

photocoagulating ocular tissue in the treatment of diseases of the eye.

The laser energy is delivered via either transpupillary delivery or intraocular endoprobe

delivery.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K113390 · printed Nov 6, 2026

Cite this page

510(k) Report. “K113390: Laser Indirect Ophthalmoscope 500(Lio-500).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113390

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026