FDA Registration Active 🇺🇸 United States

ACCELERATED CARE PLUS CORP.

Reg #: 1911273 · FEI: 1000119345 · Expires 2026
Products
9
Proprietary Names
26
Establishment Types
4
Classifications
9

Registration Details

Registration Name
ACCELERATED CARE PLUS CORP.
Registration Number
1911273
FEI Number
1000119345
Status
Active
Expiry Year
2026
Initial Importer
Yes
Address
1170 Trademark Dr Ste 104
City
RENO
State
NV
ZIP
89521
Country
US

Regulatory Submissions

510(k) Number
K945508

Owner / Operator

Firm Name
Accelerated Care Plus
Operator Number
1911273
Address
4999 Aircenter Cir, Ste 103
City
Reno
State
NV
Postal Code
89502
Country
US

Products

Device Name Product Code
Stimulator, Muscle, Powered IPF
Exerciser, Non-Measuring ION
Exerciser, Powered BXB
Stimulator, Nerve, Transcutaneous, For Pain Relief GZJ
Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat IMG
Device, Biofeedback HCC
Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat IMJ
Electrode, Cutaneous GXY
Exerciser, Non-Measuring For Stroke Rehabilitation PKS

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 ACP High Conductivity Electrodes - 2x4 ACP High Conductivity Electrodes - 2x2 ACP High Conductivity Electrodes - 4x4 ACP High Conductivity Electrodes - 3x5 Synchrony Electrodes Pharyngeal sEMG Synchrony Electrodes, Face and Neck with snap Synchrony Electrodes Oro-Facial sEMG OmniStand

Establishment Types

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