# Aesthetic Lasers, Inc.

- Location (FDA's records): Annapolis, MD
- FDA decisions: 1 (1996–1996): 1 510(k) clearance
- Product codes: GFE (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
- K963204: DMS-1000C Dermoabrader (Dec 9, 1996)

Source page: https://510kreport.com/company/aesthetic-lasers