HomeSwitzerlandMeridian Co., Ltd.

Meridian Co., Ltd.

Switzerland · Thun
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Singapore, Australia, Israel — 6 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
1listed device types
Class I 0Class II 1Class III 0
plus 3 registration records and 13 510(k), 7 PMA
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
2 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
3active device licences
Class III 3
5 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
3device registrations
CLASS C 3
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States3 registration records, 13 510(k), 7 PMA, 17 excluded
Brazil0 confirmed, 6 excluded
Canada3 confirmed, 3 excluded
Manufacturer names merged into this page: MERIDIAN AG · MERIDIAN CO., LTD.

Company information

Country
Switzerland
City
Thun

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12000
12001
22002
12003
12005
12007
12008
12011
12012
12017
12023
12024

FDA listed device types

Laser, Ophthalmic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK232417MR Q; MR Q SUPINE; MR Q SLT2024-01-25
USK231011Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse2023-09-12
USK160677MICRORUPTOR 62017-05-19
CA24885MICRORUPTOR VClass III
CA26810MERILITE OPHTHALMIC LASERClass III
CA79045MICRORUPTOR VClass III

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