FDA applicant

Skin Deep, Inc.

Philadelphia, PA2 decisions1988–19910 recalls

FDA records 2 decisions for Skin Deep, Inc. (Philadelphia, PA) from 1988 to 1991: 2 510(k) clearances. All are in product code KCW (Epilator, High Frequency, Needle-Type). 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 Skin Deep, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Skin Deep, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Skin Deep, 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 “Skin”

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

Skin Saver Systems, Inc. 1 Skin Care Management, Inc. 1 The Skin Care Centre 1

Skin Deep, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Skin”