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Data / Medical devices / United States / MDD Options, LLC

MDD Options, LLC: FDA-registered device maker in New Hill, NC, United States, 1 PMA approval

MDD Options, LLC is registered with the FDA (registration 3040937533) in New Hill, NC, United States. It lists 7 device types. The FDA files 1 PMA approval under its listings, the newest dated September 9, 2025. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3040937533
Address
355 Cedar Lane Farm Ln, New Hill, NC, United States, 27562
Owner or operator
MDD Options, LLC (10094112)
Roles
Complaint file establishment
First device listed
January 5, 2026
Registered through
2027
Brand names listed
Bio-Gram Microscope Slide, ColorJet Nano, Crystal-Violete JetDye-AF, Etzel, FixOstar, FixOstar - Hema, Giemsa JetDye-AF, Gram-Polychrom JetDye-AF Kit and more

Devices it lists

DeviceProduct codeClassRoleSource
Barrier, Absorbable, AdhesionMCN3Complaint file establishmentaccessdata.fda.gov
Romanowsky StainsGJL1Complaint file establishmentaccessdata.fda.gov
Slide Stainer, AutomatedKPA1Complaint file establishmentaccessdata.fda.gov
Slides, MicroscopeKEW1Complaint file establishmentaccessdata.fda.gov
Spinner, Slide, AutomatedGKJ1Complaint file establishmentaccessdata.fda.gov
Stains, Chemical SolutionLED1Complaint file establishmentaccessdata.fda.gov
Stains, MicrobiologicJTS1Complaint file establishmentaccessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
September 9, 2025P240015Womed Leaf Resorbable Adhesion BarrierMCN3October 25, 2026accessdata.fda.gov

Compare with other makers

Updated October 25, 2026. 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.