510(k) Report

FDA applicant

Nexxt Medical, Inc.

Chesterland, OH1 decision2010–20100 recalls

FDA records 1 decision for Nexxt Medical, Inc. (Chesterland, OH) in 2010: 1 510(k) clearance. All are in product code KWQ (Appliance, Fixation, Spinal Intervertebral Body). 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 Nexxt Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010: 1
2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Nexxt Medical, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KWQAppliance, Fixation, Spinal Intervertebral Body1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K091936Blade Anterior Cervical Plate SystemNexxt Medical, Inc. · 20102cite it

What has FDA decided for it lately?

  • K091936Blade Anterior Cervical Plate SystemNexxt Medical, Inc. · 2010

The one decision as Nexxt Medical, Inc. →

Other applicant names beginning “Nexxt”

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

Nexxt Spine, LLC 24