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ACCELERATED CARE PLUS CORP.

USA · Reno

✓ 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

9listed device types

Class I 3Class II 6Class III 0

plus 8 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 States8 registration records, 4 510(k), 0 PMA, 2 excluded

Manufacturer names merged into this page: ACCELERATED CARE PLUS CORP.

FDA 510(k) clearances by year

12006 · K060191

12009 · K093600

22016 · K153559

FDA listed device types

showing 8 of 9

Exerciser, Non-Measuring 1Exerciser, Non-Measuring For Stroke Rehabilitation 1Exerciser, Powered 1Stimulator, Muscle, Powered 1Electrode, Cutaneous 1Stimulator, Nerve, Transcutaneous, For Pain Relief 1Device, Biofeedback 1Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K153559	OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System	2016-08-26
US	K153456	Megapulse III Shortwave Diathermy	2016-06-14
US	K093600	OMNISTIM CONTINENCE+ PELVIC FLOOR STIMULATION SYSTEM	2009-12-04

ACCELERATED CARE PLUS CORP.

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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