510(k) Report

FDA applicant

Revelle Aesthetics, Inc.

Mountain View, CA2 decisions2022–20230 recalls

FDA records 2 decisions for Revelle Aesthetics, Inc. (Mountain View, CA) from 2022 to 2023: 2 510(k) clearances. All are in product code OUP (Powered Surgical Instrument For Improvement In…). Its devices cite 3 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 Revelle Aesthetics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2022: 12023: 1
2022high 1 (2022) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Revelle Aesthetics, Inc. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Which product codes does it file in?

  • OUPPowered Surgical Instrument For Improvement In The Appearance Of Cellulite2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K221336AvéliRevelle Aesthetics, Inc. · 20221cites it

What has FDA decided for it lately?

  • K232153AvéliRevelle Aesthetics, Inc. · 2023
  • K221336AvéliRevelle Aesthetics, Inc. · 2022

All 2 as Revelle Aesthetics, Inc. →