HomeIndiaSyrma Johari MedTech Limited

Syrma Johari MedTech Limited

India · Jodhpur
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 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
20listed device types
Class I 3Class II 17Class III 0
plus 24 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
6active device licences
Class II 6
16 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
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 States24 registration records, 1 510(k), 0 PMA
Canada6 confirmed, 0 excluded
Manufacturer names merged into this page: Syrma Johari MedTech Limited · SYRMA JOHARI MEDTECH LIMITED

Company information

Country
India
City
Jodhpur

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

12025 · K251594

FDA listed device types

showing 8 of 20
Electrosurgical, Cutting & Coagulation & Accessories 1Lamp, Infrared, Therapeutic Heating 1Stimulator, Muscle, Powered 1Stimulator, Neuromuscular, External Functional 1Stimulator, Nerve, Transcutaneous, Over-The-Counter 1Stimulator, Transcutaneous Electrical, Aesthetic Purposes 1Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety 1Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK251594truFlex2025-08-28
CA86883STIM2Class II
CA86884STIM4Class II
CA86746TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR & CRANIAL ELECTRICAL NERVE STIMULATORClass II

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