510(k) Report

FDA applicant

Perseus Althetics,Llc

Washington, DC1 decision2010–20100 recalls

FDA records 1 decision for Perseus Althetics,Llc (Washington, DC) in 2010: 1 510(k) clearance. All are in product code LZW (Monitor, Spine Curvature). Its devices cite 2 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

How often FDA has decided Perseus Althetics,Llc’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 — Perseus Althetics,Llc 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?

  • LZWMonitor, Spine Curvature1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K093553PosturetekPerseus Althetics,Llc · 2010

The one decision as Perseus Althetics,Llc →