Medical Device Manufacturer · US , Los Angeles , CA

Sleepcare, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026

Recent clearances: Daybreak Impression Material

1
Total
1
Cleared
0
Denied

Sleepcare, LLC has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Sleepcare, LLC

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