Denmat Holding, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Denmat Holding, LLC - FDA 510(k) Cleared Devices
Recent clearances: DenMat Multilayered Zirconia Disc, DenMat Glutaraldehyde Desensitizer
2
Total
2
Cleared
0
Denied
Denmat Holding, LLC has 2 FDA 510(k) cleared medical devices. Based in Lompoc, US.
Latest FDA clearance: Aug 2025. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Denmat Holding, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Denmat Holding, LLC
2 devices