HomeChinaKONTOUR (XI'AN) MEDICAL TECHNOLOGY CO., LTD.

KONTOUR (XI'AN) MEDICAL TECHNOLOGY CO., LTD.

China · Xi'An Shaanxi
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Taiwan, South Korea, 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
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
4listed device types
Class I 1Class II 3Class III 0
plus 14 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class I 1
2 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
3valid device licences
Class I 1Class II 2
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
2active ARTG entries
IIb 2
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 States14 registration records, 1 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: KONTOUR (XI'AN) MEDICAL TECHNOLOGY CO., LTD.

Company information

Country
China
City
Xi'An Shaanxi

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

12022 · K214109

FDA listed device types

Plate, Cranioplasty, Preformed, Non-Alterable 1Cover, Burr Hole 1Plate, Bone 1Screwdriver, Skullplate 1

Registration details (sample)

MarketIdentifierNameClass / date
USK214109PEEK Patient Specific Cranial/Craniofacial Implant(PSCI)2022-10-28
BR81747150002KIT DE INSTRUMENTOS DE CIRURGIA CRANIOMAXILOFACIALClass I

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