HomeSouth AfricaXavant Technology (Pty), Ltd.

Xavant Technology (Pty), Ltd.

South Africa · Pretoria
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Canada, Taiwan, Singapore, South Korea, Australia — 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
2listed device types
Class I 1Class II 1Class III 0
plus 5 registration records and 7 510(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
0active device licences
5 including historic records
TWTaiwanTFDA
3valid device licences
Class II 3
SGSingaporeHSA SMDR
3device registrations
CLASS B 3
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
3active ARTG entries
Class I 1IIa 2
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 States5 registration records, 7 510(k), 0 PMA
Manufacturer names merged into this page: XAVANT TECHNOLOGY (PTY) LTD · XAVANT TECHNOLOGY (PTY) LTD.

Company information

Country
South Africa
City
Pretoria

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

12007
12009
12010
12011
12014
12017
12022

FDA listed device types

Medical Device Data System 1Stimulator, Nerve, Battery-Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK213049STIMPOD NMS450 Nerve Stimulator2022-10-16
USK161091STIMPOD NMS460 Nerve Stimulator2017-01-18
USK140853STIMPOD ST2-3010 NERVE STIMULATOR2014-11-06

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