HomeUSAViant San Antonio, Inc.

Viant San Antonio, Inc.

USA · San Antonio
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Taiwan — 2 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
21listed device types
Class I 10Class II 11Class III 0
plus 22 registration records and 1 510(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
TWTaiwanTFDA
2valid device licences
Class II 2
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 States22 registration records, 1 510(k), 0 PMA, 2 excluded
Brazil0 confirmed, 2 excluded
Manufacturer names merged into this page: Viant San Antonio, Inc. · SAN ANTONIO SHOE, INC.

Company information

Country
USA
City
San Antonio

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

12003 · K022448

FDA listed device types

showing 8 of 21
Apparatus, Air Handling, Bench 1Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief 1Arthroscope 1Syringe, Piston 1Drape, Surgical, Exempt 1Tubing, Noninvasive 1Platelet And Plasma Separator For Bone Graft Handling 1Orthopedic Stereotaxic Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
USK022448WATER PURIFICATION SYSTEM2003-05-28

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