# Dermacare Products, Inc.

- Location (FDA's records): Louisville, KT
- FDA decisions: 8 (1985–1988): 8 510(k) clearances
- Product codes: GEI (1), KKX (1), JOS (1), FZZ (1)
- 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
- K882494: Elan-E Disposalbe Drape (Jul 8, 1988)
- K882421: Infant Electrosurgical Dispersive Electrode (Jun 30, 1988)
- K871910: Surgitek Disposable Bipolar Cord (Jun 1, 1987)
- K863279: Surgi-Tek Tube Positioner (Sep 9, 1986)
- K863280: Dermamarker (Sep 9, 1986)
- K863278: Surgi-Wipes (Sep 2, 1986)
- K862367: Pro-Clean (Jul 8, 1986)
- K853374: Correct-a-Count (Sep 5, 1985)

Source page: https://510kreport.com/company/dermacare-products