FDA applicant

Specialty Spine Products, LLC

San Diego, CA2 decisions2006–20060 recalls

FDA records 2 decisions for Specialty Spine Products, LLC (San Diego, CA) in 2006: 2 510(k) clearances. Most are in product codes MQP (Spinal Vertebral Body Replacement Device) and MNH (Orthosis, Spondylolisthesis Spinal Fixation). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Specialty Spine Products, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Specialty Spine Products, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Specialty Spine Products, 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 “Specialty”

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

Specialty Surgical Products, Inc. 13 Specialty Ultravision, Inc. 12 Specialty Packaging Producs, Inc. 11 Specialty Medical Products Co. 4 Specialty Appliance Works, Inc. 3 Specialty Medical Industries, Inc. 3 Specialty Water Technologies 2 Specialty Fibres and Materials, Ltd. 2 Specialty Health Products, Inc. 2 Specialty Dialysis Services 1 Specialty Drives Technologies, Inc. 1 Specialty Tint 1

Specialty Spine Products, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Specialty”