Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8030988

FEI Number

3003282815

Entity Name

MERIDIAN AG

City/State/Country

THUN Bern, CH

Establishment Address

BIERIGUTSTRASSE 7, THUN Bern CH-3608, CH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MERIDIAN AG (Owner Number: 8030988)

Owner / Operator Contact Address

BIERIGUTSTRASSE 7, --, THUN, CH-NOTA CH-3608, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Merilas 532 alpha

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQF	Laser, Ophthalmic	Ophthalmic	Class 2	886.4390	2008-03-12

Official Correspondent

Nina Spicka

US Agent Details

Kevin Walls Business: Regulatory Insight, Inc. Email: kevin@reginsight.com Phone: (720) 2545756

Related Public Records

Same Entity

MERIDIAN AG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3029221947	Meridian Medical d.o.o.	Ljubljana-Sentvid, SI

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K834060	F. & F. Koenigkramer	RELIANCE OPHTHALMIC SLIT LAMP R-083	1984-02-04

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3007851054	Avedro, A Glaukos Company	Burlington, MA, US
2031962	STALLION MEDICAL, INC.	SAN DIEGO, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8030988. Last updated year: 2026. Please use registration number 8030988 when referencing this establishment in official correspondence.