Dermal Life, LLC is one of 19732 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dermal Life, LLC - FDA 510(k) Cleared Devices
Recent clearances: HYDROPERMEATE TOPICAL EMULSION, ANSWER2SKIN SUNBURN RELIEF CREAM, ANSWER2SKIN FIRST AID CREAM
1
Total
1
Cleared
0
Denied
Dermal Life, LLC has 1 FDA 510(k) cleared medical devices. Based in Fairfax, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dermal Life, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Journey Medical Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Dermal Life, LLC
1 devices