FDA applicant

Accelerated Care Plus

Reno, NV3 decisions2006–20160 recalls

FDA records 3 decisions for Accelerated Care Plus (Reno, NV) from 2006 to 2016: 3 510(k) clearances. Most are in product codes IMJ (Diathermy, Shortwave, For Use In Applying…) and KPI (Stimulator, Electrical, Non-Implantable, For…). No recall is linked to its devices.

FDA’s records also spell it “Accelerated Care Plus Corp.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Accelerated Care Plus’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Accelerated Care Plus by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Accelerated”

FDA records each applicant name separately; these may or may not be the same firm.

Accelerated Innovation, LLC 7 Accelerated Rehab Designs, Inc. 4 Accelerated Care Plus (Acp) 1

Accelerated Care Plus

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Accelerated”