FDA applicant

Alliance Partners, LLC

Avon Lake, OH10 decisions2011–20201 recall

FDA records 10 decisions for Alliance Partners, LLC (Avon Lake, OH) from 2011 to 2020: 10 510(k) clearances. Most are in product codes MAX (Intervertebral Fusion Device With Bone Graft…) and ODP (Intervertebral Fusion Device With Bone Graft…). Its devices cite 25 predicates, 6 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 Alliance Partners, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2011high 3 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

1in 2015

2011high 1 (2015) · low 0 (2011)2026

Class I Class II/III not classified

FIG. 1 — Alliance Partners, LLC by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Alliance Partners, 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 “Alliance”

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

Alliance Medical Corp. 47 Alliance Rubber Products Sdn. Bhd. 12 Alliance Pharmaceutical Corp. 2 Alliance International Co., Ltd. 2 Alliance Global Technology Co., Ltd. 2 Alliance Medical Technologies, Inc. 1 Alliance Instruments 1 Alliance Global 1 Alliance Tech Medical, Inc. 1 Alliance Medical Marketinig 1

Alliance Partners, 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 “Alliance”