# Skin Deep, Inc.

- Location (FDA's records): Philadelphia, PA
- FDA decisions: 2 (1988–1991): 2 510(k) clearances
- Product codes: KCW (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K911983: Wizard Sterilized Electroepilation Needle (Oct 15, 1991)
- K874891: Flexie the Copper Shank Needle (Jan 7, 1988)

Source page: https://510kreport.com/company/skin-deep