# Dermacare

- Location (FDA's records): Louisville, KY
- FDA decisions: 3 (1988–2006): 3 510(k) clearances
- Names in FDA's records: Dermacare (2); Dermacare, Inc. (1)
- Product codes: GEI (1), KGS (1), GEX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tyrell, Inc.: 1 (https://510kreport.com/company/tyrell)
- Radiancy (Israel), Ltd.: 1 (https://510kreport.com/company/radiancy-israel)

## Firms that cite its devices most
- Olsen Medical: 2 (https://510kreport.com/company/olsen-medical)
- Clrs Technology Corporation: 2 (https://510kreport.com/company/clrs-technology)
- Tria Beauty, Inc.: 1 (https://510kreport.com/company/tria-beauty)
- Home Skinovations, Ltd.: 1 (https://510kreport.com/company/home-skinovations)
- Clearflash Technologies, Inc.: 1 (https://510kreport.com/company/clearflash-technologies)

## Its most-cited devices
- K060653: Thermaclear (2006), cited by 5
- K884656: Disposable Bipolar Cord and Bipolar Forcep (1988), cited by 2

## Recent decisions
- K060653: Thermaclear (Oct 24, 2006)
- K893995: Dermacare Tie Holder (Aug 11, 1989)
- K884656: Disposable Bipolar Cord and Bipolar Forcep (Nov 25, 1988)

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