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Data / Medical devices / United States / Molecular Matrix

Molecular Matrix: FDA-registered device maker in Carlsbad, CA, United States, 1 510(k) clearance

Molecular Matrix is registered with the FDA (registration 3014545238) in Carlsbad, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 29, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3014545238
Address
2075 Corte del Nogal Suite E/F, Carlsbad, CA, United States, 92011
Owner or operator
Molecular Matrix (10057433)
Roles
Complaint file establishment, Manufacturer, Repackager or relabeler
First device listed
April 5, 2018
Registered through
2026
Brand names listed
Bio-Reign Bone Graft Substitute, Osteo-P Bone Graft Substitute

Devices it lists

DeviceProduct codeClassRoleSource
Filler, Bone Void, Calcium CompoundMQV2Complaint file establishment, Manufacturer, Repackager or relabeleraccessdata.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 29, 2017K170165Osteo-P Bone Graft SubstituteMQVSubstantially EquivalentMolecular Matrix, Inc.accessdata.fda.gov

Compare with other makers

Updated December 29, 2017. 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.