FDA applicant

Accelerated Innovation, LLC

Clifton, NJ7 decisions2008–20081 recall

FDA records 7 decisions for Accelerated Innovation, LLC (Clifton, NJ) in 2008: 7 510(k) clearances. Most are in product codes KWY (Prosthesis, Hip, Hemi-, Femoral…) and KWQ (Appliance, Fixation, Spinal Intervertebral Body). Its devices cite 20 predicates, 0 of them its own earlier devices. 1 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, orthopedic panel, where it files most

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

FDA decisions per year

7in 2008

2008high 7 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

1in 2015

2008high 1 (2015) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Accelerated Innovation, LLC by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Accelerated Innovation, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 Rehab Designs, Inc. 4 Accelerated Care Plus 3 Accelerated Care Plus (Acp) 1

Accelerated Innovation, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Accelerated”