# Spelna, Inc.

- Location (FDA's records): Fredericksburg, VA
- FDA decisions: 11 (1982–1986): 11 510(k) clearances
- Product codes: ELC (4), EIA (2), FLG (1), KOJ (1), DSH (1), EKZ (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
- K852525: Satalec Piezotec (Jan 30, 1986)
- K852527: Satalec Septosonic SC 80/SC 120 (Jan 3, 1986)
- K852522: Satalec Servotome (Dec 27, 1985)
- K853200: 5X2 Satalec Chiropody Case (Oct 18, 1985)
- K852521: Satlec Prophy Unit PU 3055 (Jul 31, 1985)
- K852524: Satalec Servotorque S2 SX2 (Jul 31, 1985)
- K832674: Satelec Prophy Unit PU 2000S (Mar 16, 1984)
- K832664: Satelec Suprasson Piezomatic P2 (Mar 16, 1984)

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