# Sharplan Industries, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (1986–1986): 4 510(k) clearances
- Product codes: LNK (2), GEX (1), LLO (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
- K861044: Model 2100 ND:Yag Surgical Laser Neurosurgical Ind (Oct 28, 1986)
- K861047: Model 2100 ND:Yag Surgical Laser Gastrointestinal (Jun 17, 1986)
- K861046: Model 2100 ND:Yag Surgical Laser Urological Indica (May 2, 1986)
- K861045: Model 2100 ND:Yag Surgical Laser Pulmonary Indicat (Apr 23, 1986)

Source page: https://510kreport.com/company/sharplan-industries