
Somnomed Technologies Inc., Doing Business AS Remware
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DreamClear is an FDA 510(k)-cleared medical device (K240646) manufactured by Somnomed Technologies Inc., Doing Business AS Remware. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 3, 2024. Regulation: 8.

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