FDA applicant
Mycone Dental Supply Co., Inc.
FDA records 3 decisions for Mycone Dental Supply Co., Inc. (Cherry Hill, NJ) from 2003 to 2011: 3 510(k) clearances. Most are in product codes EBG (Crown And Bridge, Temporary, Resin) and EBI (Resin, Denture, Relining, Repairing, Rebasing). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Mycone Dental Supply Co., Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Mycone Dental Supply Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Mycone”
FDA records each applicant name separately; these may or may not be the same firm.