Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1911273

FEI Number

1000119345

Entity Name

ACCELERATED CARE PLUS CORP.

City/State/Country

RENO, NV, US

Establishment Address

1170 Trademark Dr Ste 104, RENO, NV 89521, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Accelerated Care Plus (Owner Number: 1911273)

Owner / Operator Contact Address

4999 Aircenter Cir, Ste 103, Reno, NV 89502, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K153456

PMA Number

N/A

All Registered Proprietary Names

Omnistim FX2 Cycle/Walk Omnistim FX2 Portable PENS OmniME OmniVR Elite Virtual Reality Rehabilitation System OmniFlow Therapy System Synchrony Dysphagia Solutions by ACP ACPlus Respiratory Assessment OmniFlow Software OmniTour System ACPLUS Platform OmniTour Software OmniCycle Revo OmniCycle Connect Omnicycle Elite OmniCycle Elite 7 Inch Screen OmniVersa OmnisEMG OmniSWD

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2008-02-07
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2009-09-11
BXB	Exerciser, Powered	Physical Medicine	Class 1	890.5380	2008-10-07
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2016-09-09
IMG	Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat	Physical Medicine	Class 2	890.5860	2016-09-09
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2016-09-09
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2014-08-21
IMJ	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat	Physical Medicine	Class 2	890.5290	2016-06-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Accelerated Care Plus

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K030403	Cefar Medical AB	CEFAR REHAB 2 AND REHAB 2 PRO	2003-07-17
K231440	Shenzhen Roundwhale Technology Co. , Ltd.	Combo Electrotherapy Device	2023-11-03
K820884	Nitron Electronics	ELECTRICAL MUSCLE STIMULATOR	1982-04-29
K201958	Therasigma, LLC	ETD Family of Electrotherapy Devices	2020-08-04
K964028	Mettler Electronics Corp.	SYS STIM 226	1997-02-03

Similar Registrations

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3005344585	ODSTOCK MEDICAL LTD	SALISBURY Wiltshire, GB
3038295706	JUST KEEP HEALTHY CO., LTD.	Samkkei Munichay District Kampong Speu, KH
3019892999	CIONIC Facility	Scotts Valley, CA, US
3012316249	COMPASS HEALTH BRANDS (CORPORATE OFFICE)	Middleburg Heights, OH, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1911273. Last updated year: 2026. Please use registration number 1911273 when referencing this establishment in official correspondence.