HomeUSAOrthovita, Inc.

Orthovita, Inc.

USA · Malvern
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Israel — 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
26510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 26 510(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
3active device licences
Class II 2Class IV 1
4 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
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 States0 registration records, 26 510(k), 0 PMA
Canada3 confirmed, 0 excluded
Manufacturer names merged into this page: ORTHOVITA INC.

Company information

Country
USA
City
Malvern

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

21995
12000
12001
62003
22005
12007
22008
12009
22010
22011
22014
12015
22016
12017

Registration details (sample)

MarketIdentifierNameClass / date
USK163621Vitoss Bioactive (BA) Injectable2017-05-02
USK161447HydroSet XT2016-10-06
USK153608Vitoss BiModal Bone Graft Substitute Foam Strip2016-02-12
CA21399CELLPAKER PLASMA COLLECTION DEVICEClass II
CA22258VITAGELClass IV
CA72431VITAGEL SURGICAL HEMOSTAT SPRAY SETClass II

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