Prismatik Dentalcraft, Inc. - FDA 510(k) Cleared Devices
57
Total
57
Cleared
0
Denied
Prismatik Dentalcraft, Inc. has 57 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Latest FDA clearance: Jan 2026. Active since 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Prismatik Dentalcraft, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Prismatik Dentalcraft, Inc.
26 devices
Cleared
Jan 30, 2026
BruxZir® Shaded 16 PLUS
Dental
30d
Cleared
Nov 18, 2025
Inclusive® Titanium Abutments compatible with: Camlog® CONELOG® Implant...
Dental
95d
Cleared
Sep 03, 2025
BruxZir® NOW
Dental
30d
Cleared
Jun 25, 2025
Flexible Partial Resin
Dental
142d
Cleared
Mar 21, 2025
Autoclavable Cassette (Glidewell HT™ Implant Guided Surgical Kit, Glidewell...
General Hospital
205d
Cleared
Feb 25, 2025
BruxZir® Esthetic NOW
Dental
29d
Cleared
Sep 12, 2024
Glidewell™ 3DP Denture Base Resin
Dental
107d
Cleared
Jul 12, 2024
Inclusive® Titanium Abutments compatible with: Keystone® Dental PrimaConnex®,...
Dental
164d
Cleared
May 15, 2024
BruxZir® NOW SRC
Dental
320d
Cleared
May 01, 2024
BruxZir® Esthetic
Dental
30d
Cleared
Mar 20, 2024
BruxZir® Radiant
Dental
19d
Cleared
Mar 14, 2024
CloudPoint FastDesign Chairside
Dental
293d