510(k) Report

FDA applicant

Michael Todd, LP

Port St Lucie, FL1 decision2016–20160 recalls

FDA records 1 decision for Michael Todd, LP (Port St Lucie, FL) in 2016: 1 510(k) clearance. All are in product code OLP (Over-The-Counter Powered Light Based Laser For…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Michael Todd, LP’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Michael Todd, LP by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Michael”

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