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CENTRAL SOLUTIONS, INC.

USA · Kansas City

✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 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

55listed device types

Class I 35Class II 20Class III 0

plus 58 registration records and 7 510(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 3

12 including historic records

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 States58 registration records, 7 510(k), 0 PMA, 20 excluded

Brazil0 confirmed, 6 excluded

Saudi Arabia0 confirmed, 1 excluded

Canada3 confirmed, 3 excluded

Manufacturer names merged into this page: Sunset Healthcare Solutions Central Warehouse · CENTRAL ACCESS SOLUTIONS LLC · CENTRAL SOLUTIONS, INC. · CENTRAL DENTAL SOLUTIONS INC.

FDA 510(k) clearances by year

51995 · K954292

11996 · K955850

11998 · K983585

FDA listed device types

showing 8 of 55

Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature 1Apparatus, Suction, Ward Use, Portable, Ac-Powered 1Nebulizer (Direct Patient Interface) 1Bottle, Collection, Vacuum 1Apparatus, Suction, Operating-Room, Wall Vacuum Powered 1Ventilator, Continuous, Facility Use 1Oximeter 1Filter, Bacterial, Breathing-Circuit 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K983585	LOW PH PHENOLIC 256	1998-11-06
US	K955850	PRO-TECH	1996-02-09
US	K954292	Q5. 5-5.5NPB-2.5HW	1995-09-27
CA	12594	ACCUQUIP LATEX MEDICAL EXAMINATION GLOVES	Class II
CA	91321	VIRTA NITRILE MEDICAL EXAMINATION GLOVE	Class II
CA	100134	VIRTA LATEX POWDER FREE EXAM GLOVES	Class II

CENTRAL SOLUTIONS, INC.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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