510(k) Report

FDA applicant

Mycone Dental Supply Co., Inc.

Cherry Hill, NJ3 decisions2003–20110 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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

2010: 12011: 1
2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mycone Dental Supply Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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Other applicant names beginning “Mycone”

FDA records each applicant name separately; these may or may not be the same firm.