HomeUSACartiva, Inc.

Cartiva, Inc.

USA · Alpharetta
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Canada, Israel — 4 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
3510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 3 510(k), 16 PMA
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class I 1
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 II 1Class III 1
3 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
2registrations
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, 3 510(k), 16 PMA
Brazil1 confirmed, 0 excluded
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: CARTIVA, INC.

Company information

Country
USA
City
Alpharetta

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

12014 · K142490
12018 · K181348
12019 · K192156

Registration details (sample)

MarketIdentifierNameClass / date
USK192156Cartiva SCI instrumentation set2019-09-04
USK181348Cartiva SCI Disposable Instrumentation Set2018-06-20
USK142490ProxiFuse Hammer Toe Device2014-12-15
BR81528780002INSTRUMENTAÇÃO SCI CARTIVA TMClass I
CA68429CARTIVA SYNTHETIC CARTILAGE IMPLANTClass III
CA101341METATARSAL DISPOSABLE INSTRUMENT SETClass II

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