HomeUSAMed Way, Inc.

Med Way, Inc.

USA · Buford
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 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
10listed device types
Class I 8Class II 2Class III 0
plus 10 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
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 States10 registration records, 1 510(k), 0 PMA, 19 excluded
Brazil2 confirmed, 4 excluded
Saudi Arabia0 confirmed, 1 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: MED WAY INC. · Fuzhou Best Way Med-Macromolecule Co., Ltd.

Company information

Country
USA
City
Buford

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

12024 · K241023

FDA listed device types

showing 8 of 10
Negative Pressure Wound Therapy Powered Suction Pump 1Mattress, Air Flotation, Alternating Pressure 1Silicone Hydrogel For Scar Management 1Device, Intravascular Catheter Securement 1Dressing, Wound, Hydrophilic 1Tape And Bandage, Adhesive 1Gauze / Sponge,Nonresorbable For External Use 1Elastomer, Silicone, For Scar Management 1

Registration details (sample)

MarketIdentifierNameClass / date
USK241023Negative Pressure Wound Therapy Device (V-Move, V-Grand)2024-08-19
BR10150470288CATETER FEP IV PERIFÉRICO DE SEGURANÇA SISTEMA FECHADO SAFERClass II
BR10150470299CATETER PU IV PERIFÉRICO DE SEGURANÇA SISTEMA FECHADO SAFER PLUSClass II

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