FDA applicant

Accelerated Care Plus (Acp)

Reno, NV1 decision2016–20160 recalls

FDA records 1 decision for Accelerated Care Plus (Acp) (Reno, NV) in 2016: 1 510(k) clearance. All are in product code IMG (Stimulator, Ultrasound And Muscle, For Use In…). No recall is linked to its devices.

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 (Acp)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Accelerated Care Plus (Acp) by year, 2016–2026Sources: 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 3

Accelerated Care Plus (Acp)

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Accelerated”