FDA applicant

Acme Spine, LLC

Riverside, CA2 decisions2000–20070 recalls

FDA records 2 decisions for Acme Spine, LLC (Riverside, CA) from 2000 to 2007: 2 510(k) clearances. Most are in product codes MNH (Orthosis, Spondylolisthesis Spinal Fixation) and MNI (Orthosis, Spinal Pedicle Fixation). 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, orthopedic panel, where it files most

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

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Acme”

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

Acme United Corp. 27 Acme Medical Scale Co. 10 Acme-Monaco Corp. 5 Acme Filter Mask, Inc. 1 Acme Medical, Inc. 1 Acme Automatic Disposable 1 Acme Portable Machines, Inc. 1

Acme Spine, LLC

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Acme”