Meridian AG
THUN Bern, CH
MERIDIAN AG appears in FDA device records in THUN Bern, CH. FDA records list 13 510(k) clearances between and , 7 PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 13 510(k) clearances for Meridian AG between 2000 and 2024. The busiest year on record is 2002, with 2. The most recent is 2024, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 1 |
| 2001 | 1 |
| 2002 | 2 |
| 2003 | 1 |
| 2005 | 1 |
| 2007 | 1 |
| 2008 | 1 |
| 2011 | 1 |
| 2012 | 1 |
| 2017 | 1 |
| 2023 | 1 |
| 2024 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K232417 | MR Q; MR Q SUPINE; MR Q SLT | HQF | Substantially Equivalent | |
| K231011 | Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse | HQF | Substantially Equivalent | |
| K160677 | MICRORUPTOR 6 | GEX | Substantially Equivalent | |
| K113390 | LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500) | GEX | Substantially Equivalent | |
| K102375 | LUCIA | ILY | Substantially Equivalent | |
| K081962 | LAPEX BCS | ILY | Substantially Equivalent | |
| K072823 | MERILAS 532A | HQF | Substantially Equivalent | |
| K034009 | LAPEX 2000 | NHN | Substantially Equivalent | |
| K023238 | MCPULSE | JOM | Substantially Equivalent | |
| K023045 | MICRORUPTER V | LXS | Substantially Equivalent | |
| K020360 | ABR-2000 | GZO | Substantially Equivalent | |
| K010897 | MERIDIAN-PORTABLE | GZO | Substantially Equivalent | |
| K001347 | MERIDIAN-II AND MERDIAN-PLUS | GZO | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 8030988 | 3003282815 | MERIDIAN AG | BIERIGUTSTRASSE 7, THUN Bern CH-3608 CH | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- GZODevice, Galvanic Skin Response Measurement
- ILYLamp, Infrared, Therapeutic Heating
- LXSLaser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla
- LOILaser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
- HQFLaser, Ophthalmic
- JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic
- GEXPowered Laser Surgical Instrument
- NHNPowered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Meridian AG edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain