510(k) Report

FDA applicant

Medicis Technologies Corporation

Washington, DC2 decisions2011–20110 recalls

FDA records 2 decisions for Medicis Technologies Corporation (Washington, DC) in 2011: 2 510(k) clearances. All are in product code OHV (Focused Ultrasound For Tissue Heat Or…). Its devices cite 2 predicates, 1 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 Medicis Technologies Corporation’s devices, and how often a recall has named them.

FDA decisions per year

2in 2011

2011: 2
2011high 2 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Medicis Technologies Corporation by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OHVFocused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 1 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.

  • K112626Lipsonix (R) System Model 2Medicis Technologies Corporation · 20113cite it
  • K100874Liposonix System, Model 1 P00XXXXMedicis Technologies Corporation · 20111cites it

What has FDA decided for it lately?

  • K112626Lipsonix (R) System Model 2Medicis Technologies Corporation · 2011
  • K100874Liposonix System, Model 1 P00XXXXMedicis Technologies Corporation · 2011

All 2 as Medicis Technologies Corporation →