Crystal Mark, Inc. is one of 12904 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crystal Mark, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ABRADENT MICRO ABRASIVE SANDBLASTER MODEL DV-1
1
Total
1
Cleared
0
Denied
Crystal Mark, Inc. has 1 FDA 510(k) cleared medical devices. Based in Encinitas, US.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Crystal Mark, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Crystal Mark, Inc.
1 devices