510(k) Report

FDA applicant

Esthetic Education, LLC

Scottsdale, AZ1 decision2020–20200 recalls

FDA records 1 decision for Esthetic Education, LLC (Scottsdale, AZ) in 2020: 1 510(k) clearance. All are in product code QAI (Powered Microneedle Device). Its devices cite 1 predicate, 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 Esthetic Education, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Esthetic Education, LLC by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Esthetic Education, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • QAIPowered Microneedle Device1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K200044SkinStylus SteriLock MicroSystemEsthetic Education, LLC · 20201cites it

What has FDA decided for it lately?

  • K200044SkinStylus SteriLock MicroSystemEsthetic Education, LLC · 2020

The one decision as Esthetic Education, LLC →

Other applicant names beginning “Esthetic”

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

Esthetic Medical, Inc. 2