HomeUSAVertebral Technologies, Inc.

Vertebral Technologies, Inc.

USA · Plymouth
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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
7510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 7 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
5registered devices
Class I 5
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
2active device licences
Class III 2
TWTaiwanTFDA
0valid device licences
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 States0 registration records, 7 510(k), 0 PMA, 1 excluded
Brazil5 confirmed, 0 excluded
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: VERTEBRAL TECHNOLOGIES, INC. · VTI - Vertebral Technologies, Inc.

Company information

Country
USA
City
Plymouth

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

12008 · K080673
22009 · K093675
12010 · K102277
22011 · K110226
12013 · K131540

Registration details (sample)

MarketIdentifierNameClass / date
USK131540INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE2013-09-03
USK110226INTERFUSE T INVERTEBRAL BODY FUSION DEVICE2011-05-27
USK110045INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE2011-02-03
BR10355870204Instrumentos VTI ANCClass I
BR10355870205Instrumentos VTI NANCClass I
BR10355870211Instrumentos VTI NACClass I
CA83225INTERFUSE S INTERVERTEBRAL BODY FUSION DEVICEClass III
CA90448INTERFUSE T SYSTEMClass III

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