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Data / Medical devices / United States / Microcopy, Division Of Neo-Flo, Inc.

Microcopy, Division Of Neo-Flo, Inc.: FDA-registered device maker in Kennesaw, GA, United States, 1 510(k) clearance

Microcopy, Division Of Neo-Flo, Inc. is registered with the FDA (registration 2023633) in Kennesaw, GA, United States. It lists 8 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 10, 1989. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2023633
FEI number
1000111927
Address
3120 Moon Station Road NW, Kennesaw, GA, United States, 30144
Owner or operator
MICROCOPY, DIV. NEO-FLO, INC. (2023633)
Roles
Complaint file establishment, Manufacturer
First device listed
June 16, 1992
Registered through
2026
Brand names listed
Cut Carbide, Flaps, Gazelle, Minnow, NeoBurr, NeoDiamond, NeoDiamond IPR Strips, NeoDrys and more

Devices it lists

DeviceProduct codeClassRoleSource
Absorber, Saliva, PaperKHR1Complaint file establishment, Manufactureraccessdata.fda.gov
Bur, DentalEJL1Complaint file establishment, Manufactureraccessdata.fda.gov
Disk, AbrasiveEHJ1Complaint file establishment, Manufactureraccessdata.fda.gov
Holder, Film, X-RayEGZ1Complaint file establishment, Manufactureraccessdata.fda.gov
Instrument, Diamond, DentalDZP1Complaint file establishment, Manufactureraccessdata.fda.gov
Point, AbrasiveEHL1Complaint file establishment, Manufactureraccessdata.fda.gov
Strip, Polishing AgentEHM1Complaint file establishment, Manufactureraccessdata.fda.gov
Wheel, Polishing AgentEJQ1Complaint file establishment, Manufactureraccessdata.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
March 10, 1989K890734DRY TIPSKHRSubstantially EquivalentMicrocopy, Div. Neo-Flo, Inc.accessdata.fda.gov

Compare with other makers

Updated March 10, 1989. 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.