510(k) Report

FDA applicant

Spinal Specialties, Inc.

San Antonio, TX8 decisions1994–19962 recalls

FDA records 8 decisions for Spinal Specialties, Inc. (San Antonio, TX) from 1994 to 1996: 8 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Spinal Specialties, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Spinal Specialties, Inc. since 2007.

Recalls per year

2in 2016

2016: 2
2007high 2 (2016) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Spinal”

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