HomeUSAMettler Electronics Corporation

Mettler Electronics Corporation

USA · Anaheim
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Saudi Arabia, Canada, Taiwan, Singapore, 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
15listed device types
Class I 2Class II 13Class III 0
plus 15 registration records and 34 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
2registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
7active device licences
Class II 6Class III 1
16 including historic records
TWTaiwanTFDA
2valid device licences
Class II 2
SGSingaporeHSA SMDR
1device registrations
CLASS B 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
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 States15 registration records, 34 510(k), 0 PMA
Saudi Arabia2 confirmed, 0 excluded
Canada7 confirmed, 0 excluded
Manufacturer names merged into this page: METTLER ELECTRONICS CORP. · Mettler Electronics Corp

Company information

Country
USA
City
Anaheim

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

11987
31988
31989
11993
31994
11995
11997
21999
12001
12002
22003
12004
12005
12006
12007
12009
12011
12012
12023
12024

FDA listed device types

showing 8 of 15
Lamp, Infrared, Therapeutic Heating 1Stimulator, Nerve, Transcutaneous, Over-The-Counter 1Stimulator, Muscle, Powered 1Stimulator, Neuromuscular, External Functional 1Electrode, Cutaneous 1Interferential Current Therapy 1Stimulator, Muscle, Powered, For Muscle Conditioning 1Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat 1

Registration details (sample)

MarketIdentifierNameClass / date
USK233926accufit2024-03-21
USK223802accufit2023-10-06
USK113017SYS*STIM 2402012-06-26
SAME0000001356SFDAA00001G5 Massage Units
SAME0000001356SFDAA00001G5 Massage Units
CA1188SONICATOR PLUSClass II
CA1412SONICATOR ULTRASOUND GENERATORClass II
CA66505SILBERG T.P.S. - TISSUE PREPARATION SYSTEMClass II

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