# Derma-Lase Co.

- Location (FDA's records): Hopkinton, MA
- FDA decisions: 5 (1992–1993): 5 510(k) clearances
- Product codes: GEX (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sharplan Lasers, Inc.: 1 (https://510kreport.com/company/sharplan-lasers)

## Its most-cited devices
- K924647: DLR-1 Derma-Lase Ruby Laser/DLR-1/Derma-Lase Syst (1993), cited by 1

## Recent decisions
- K932156: Multiline; Dly-1 (Oct 15, 1993)
- K930975: Derma-Lase Dla-1 Laser (Aug 19, 1993)
- K930793: Multiline; Dly-1 (Aug 19, 1993)
- K924647: DLR-1 Derma-Lase Ruby Laser/DLR-1/Derma-Lase Syst (Jun 4, 1993)
- K913256: Derma-Lase Ruby Laser - Model DLR-1 (Jan 22, 1992)

Source page: https://510kreport.com/company/derma-lase