HomeUSAVesta, Inc.

Vesta, Inc.

USA · Franklin
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
10listed device types
Class I 3Class II 3Class III 3unclassified 1
plus 11 registration records and 4 510(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
pendingnot queried
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 States11 registration records, 4 510(k), 0 PMA
Brazil0 confirmed, 1 excluded
Manufacturer names merged into this page: VESTA

Company information

Country
USA
City
Franklin

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

11979 · K792018
11980 · K792719
11981 · K810960
11983 · K834078

FDA listed device types

showing 8 of 10
Electrosurgical, Cutting & Coagulation & Accessories 1Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue 1Tubes, Gastrointestinal (And Accessories) 1Instrument, Ultrasonic Surgical 1Stimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy 1Stimulator, Spinal-Cord, Totally Implanted For Pain Relief 1Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation 1Orthopedic Manual Surgical Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
USK834078SILICONE RUGGER DISPOSABLE YOKE-CPAP1983-12-27
USK810960NASOPHARYNGEAL AIRWAY1981-04-23
USK7927193 WAY URETHRAL IRRIGATION CATHETER1980-01-16

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