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ACCELERATED CARE PLUS CORP.

Last updated September 17, 2026

Information

Country: US
Address: 1170 Trademark Dr Ste 104, RENO, NV, 89521
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000119345
DUNS Number: —

Catalogue (40)

Device	Model / Reference	Registries	Class	Status
Synchrony Oro-Facial sEMG Electrode	61879	FDA UDI	Class II	Active
OmniTour	OmniTourSoftware	FDA UDI	Class I	Active
Ultraphonic (250ml Bottle)	45539	FDA UDI	Class II	Unknown
ACP High Conductivity Electrodes 3x5	26854	FDA UDI	Class II	Active
Neuroprobe 500 Pro	140500B	FDA UDI	Class II	Active
Omnistim FX2 Continence Plus Portable	300100A	FDA UDI	Class II	Unknown
OmniVersa High Conductivity Electrodes	26124	FDA UDI	Class II	Active
OmniStim FX2 Portable PENS	300200A-1	FDA UDI	Class II	Unknown
Omnistim FX2 Cycle/Walk Portable	300400A	FDA UDI	Class II	Active
Omnipad Light Therapy, Dual 5x7 Pads	76896	FDA UDI	Class II	Active
Megapulse II	1903029	FDA UDI	Class II	Unknown
OmniME	100MTS	FDA UDI	Class I	Active
OmnisEMG	44144	FDA UDI	Class II	Active
Omnistim FX2 Pro Sport	100FX2D	FDA UDI	Class II	Unknown
OmniFlow Therapy System	100FLO	FDA UDI	Class I	Active
OmniTour System	300800T	FDA UDI	Class I	Active
OmniVR Elite	300600C	FDA UDI	Class I	Active
Megapulse III/OmniSWD	1903030	FDA UDI	Class II	Active
ACPlus Platform	100ACPLUS	FDA UDI	Class I	Active
Electrodes Pharyngeal sEMG	34184	FDA UDI	Class II	Active
Omnistim FX2 Portable	300200A	FDA UDI	Class II	Active
OmniVersa	100FXF	FDA UDI	Class II	Active
Synchrony Dysphagia Solutions by ACP	300800A	FDA UDI	Class II	Active
OmniCycle Elite 7 Inch Screen Motorized Therapeutic Exercise System	A007-533	FDA UDI	Class I	Active
ACP High Conductivity Electrodes 2X4	21227	FDA UDI	Class II	Active
ACP High Conductivity Electrodes 2X2	38155	FDA UDI	Class II	Active
Omnisound 3000E	1203000E	FDA UDI	Class II	Active
Synchrony Face & Neck PENS Electrode	74921	FDA UDI	Class II	Active
OmniVersa High Conductivity Electrodes	26135	FDA UDI	Class II	Active
OmniVersa High Conductivity Electrodes	26122	FDA UDI	Class II	Active
Omnistim 500 Pro	100500C	FDA UDI	Class II	Active
Ultraphonic, 5 Liter w/ bottle	32060	FDA UDI	Class II	Unknown
ACPlus Respiratory Assessment	ARASoftware	FDA UDI	Class I	Active
ACP High Conductivity Electrodes 4x4 electrodes	40944	FDA UDI	Class II	Active
OmniFlow Software	FlowSoftware	FDA UDI	Class I	Active
Omnistim FX2 Pro	100FX2C	FDA UDI	Class II	Unknown
Omnistim Continence+ Pelvic Floor Stimulation System	K093600	FDA 510(k)	Class II	Active
Megapulse III Shortwave Diathermy	K153456	FDA 510(k)	Class II	Active
OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy System	K153559	FDA 510(k)	Class II	Active
Acp Omnipad Light Therapy System & Acp Omnipad 500 Control Unit	K060191	FDA 510(k)	Class II	Active

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 25, 2021	Z-2518-2021	—	open, classified	Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health
Jun 12, 2013	Z-1837-2013	—	terminated	An anomaly in the firmware that may cause Omnicycle Elite to operate at a speed other than what was previously set when in reverse mode.