HomeUSARenal Solutions, Inc.

Renal Solutions, Inc.

USA · Warrendale
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Canada, Australia — 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
1listed device types
Class I 0Class II 1Class III 0
plus 6 registration records and 12 510(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
1active device licences
Class III 1
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIb 1
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 States6 registration records, 12 510(k), 0 PMA, 17 excluded
Canada1 confirmed, 4 excluded
Manufacturer names merged into this page: RENAL CARE DIALYSIS SOLUTIONS, S.A. DE C.V. · Nipro Renal Solutions USA, Corporation · RENAL SOLUTIONS INC.

Company information

Country
USA
City
Warrendale

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
12005
12006
12007
22010
12011
12012
12013
12020
22023

FDA listed device types

Dialysate Concentrate For Hemodialysis (Liquid Or Powder) 1

Registration details (sample)

MarketIdentifierNameClass / date
USK223431Citric Complete Liquid Citric Acid Concentrate2023-08-04
USK221652NIKKICART2023-03-03
USK193155Nipro Dry Complete Dry Acid Concentrate for Hemodialysis2020-11-25
CA70920ALLIENT SORBENT HEMODIALYSIS SYSTEMClass III

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