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Data / Medical devices / United States / Crystalmark Dental Systems, Inc.

Crystalmark Dental Systems, Inc.: FDA-registered device maker in Glendale, CA, United States, 1 510(k) clearance

Crystalmark Dental Systems, Inc. is registered with the FDA (registration 2029314) in Glendale, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 31, 1996. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2029314
FEI number
1000306507
Address
621 Ruberta Ave., Glendale, CA, United States, 91201
Owner or operator
CRYSTALMARK DENTAL SYSTEMS, INC. (9031606)
Roles
Manufacturer
First device listed
October 30, 1997
Registered through
2026
Brand names listed
Abrasion Resistant Mirror, Crystalair

Devices it lists

DeviceProduct codeClassRoleSource
AirbrushKOJ2Manufactureraccessdata.fda.gov
Mirror, MouthEAX1Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 31, 1996K964145ABRADENT MICRO ABRASIVE SANDBLASTER MODEL DV-1KOJSubstantially EquivalentCrystal Mark, Inc.accessdata.fda.gov

Compare with other makers

Updated December 31, 1996. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.