FDA applicant

Wellquest Intl., Inc.

New York, NY2 decisions1997–20140 recalls

FDA records 2 decisions for Wellquest Intl., Inc. (New York, NY) from 1997 to 2014: 2 510(k) clearances. Most are in product codes KCX (Epilator, High Frequency, Tweezer-Type) and OHT (Light Based Over-The-Counter Hair Removal). 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 Wellquest Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 1 (2014) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wellquest Intl., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wellquest Intl., Inc.’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

Other applicant names beginning “Wellquest”

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

Wellquest International, Inc. 1

Wellquest Intl., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Wellquest”