Medical Device Manufacturer · US , Bozeman , MT

Neuralynx, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011
2
Total
2
Cleared
0
Denied

Neuralynx, Inc. has 2 FDA 510(k) cleared medical devices. Based in Bozeman, US.

Latest FDA clearance: Apr 2025. Active since 2011. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Neuralynx, Inc. Filter by specialty or product code using the sidebar.

2 devices
1–2 of 2
Atlas Stim Headbox (NK) (31-0601-0077); Atlas Stim Headbox (Touchproof) (31-0601-0089); Atlas Stim Headbox (HD) (31-0601-0132); ASHB FIBER OPTIC DUPLEX CONN 2m (31-0204-0001); ASHB FIBER OPTIC DUPLEX CONN 7m (31-0204-0002); ATLAS Stim Headbox Software (36-0301-0006); Atlas Headbox Interface Cable (NK) (31-0204-003); Atlas Headbox Interface Cable (Touchproof) (31-0204-004); Atlas Headbox Interface Cable (HD) (31-0204-005); Atlas Headbox Expansion Panel (31-0607-0014)
K250094 · GYC Electrode, Cortical · Neurology
Apr 2025 90d
ENTERPRISE ELECTROPHYSIOLOGY SYSTEM
K110967 · OMC Reduced- Montage Standard Electroencephalograph · Neurology
Jun 2011 85d
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