# Somnitec, Inc.

- Location (FDA's records): Van Nuys, CA
- FDA decisions: 4 (1991–1991): 4 510(k) clearances
- Product codes: GXY (1), LEL (1), DRX (1), BZG (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
- K911989: Gold Cup Eeg Cutaneous Electrode W/Lead and Ext. (Jul 30, 1991)
- K912817: Somnimic (R) (Jul 26, 1991)
- K912234: Somniprobe (R) Model Number 10093, Modification (Jul 22, 1991)
- K911990: Ecg Female-to-Pin Snap Electrode W/Leads and Ext. (Jun 21, 1991)

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