Skip to content

Meridian AG

Also registered as Meridian Co., Ltd.

Country not established FDA

Devices
13
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Meridian AG makes

Meridian AG manufactures ophthalmic laser systems, including indirect ophthalmoscopes with integrated laser capabilities (e.g., the LIO-500) and selective laser devices for treating ocular conditions. Their portfolio includes Nd:YAG laser systems (e.g., Microruptor MR-2) for posterior segment procedures and short-pulse lasers (e.g., Merilas 532A, Merilas 532/577/810 shortpulse) for selective tissue ablation. Additional devices like the Microruptor V and MR Q series (including supine and SLT variants) are designed for glaucoma and cataract surgeries.

The company’s devices are regulated under FDA pathways, with Class II and Class III classifications requiring 510(k) or PMA clearance. These products are listed in the FDA’s 510(k) and PMA registries, reflecting their authorised status for commercial distribution in the US. Meridian AG is headquartered in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

Search and filter all 13 devices
Skip device list

  • Lapex 2000 Ref K034009

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Laser Indirect Ophthalmoscope 500(Lio-500) Ref K113390

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Microrupter V Ref K023045

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Meridian-Ii And Merdian-Plus Ref K001347

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Mr Q; Mr Q Supine; Mr Q Slt Ref K232417

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Abr-2000 Ref K020360

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse Ref K231011

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Lucia Ref K102375

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Lapex Bcs Ref K081962

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Meridian-Portable Ref K010897

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Merilas 532A Ref K072823

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Mcpulse Ref K023238

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Microruptor Mr-2 Nd:yag Laser System Ref K160677

    Active Regimes: PMA 510(k) Registry: PMA Class:III

Rows 1-13 of 13

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Meridian AG THUN Bern · CH FEI 3003282815

Frequently asked questions

How many devices does Meridian AG have in the registry?

The registry currently lists 13 devices for Meridian AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Meridian AG's devices?

Among its 13 most recently registered devices, Meridian AG has devices listed in FDA 510(k) (12 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Meridian AG's devices fall under?

Among its 13 most recently registered devices, the classes recorded for Meridian AG's devices are Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Meridian AG in the registry?

The most recently registered devices listed for Meridian AG include LAPEX 2000, LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500), MICRORUPTER V and MERIDIAN-II AND MERDIAN-PLUS.

Which FDA establishments are linked to Meridian AG?

1 FDA establishment is linked to Meridian AG in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.