Cristaline Aligners GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Cristaline Aligners GmbH - FDA 510(k) Cleared Devices
Recent clearances: Cristaline Aligners Z FLX
1
Total
1
Cleared
0
Denied
Cristaline Aligners GmbH has 1 FDA 510(k) cleared medical devices. Based in Pforzheim, DE.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Cristaline Aligners GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Trisler Consulting (Dba) as regulatory consultant.
FDA 510(k) Regulatory Record - Cristaline Aligners GmbH
1 devices