Medtek Skincare, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtek Skincare, LLC - FDA 510(k) Cleared Devices
Recent clearances: Poly Clear, POLY REJUV
2
Total
2
Cleared
0
Denied
Medtek Skincare, LLC has 2 FDA 510(k) cleared medical devices. Based in Hudson, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medtek Skincare, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Aegis Regulatory, Inc. and FDA Regulatory Consultants, LLC.
FDA 510(k) Regulatory Record - Medtek Skincare, LLC
2 devices