FDA applicant
Dmp, Ltd.
FDA records 9 decisions for Dmp, Ltd. (Markopoulo, Attiki, GR) from 1989 to 2012: 9 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and EBF (Material, Tooth Shade, Resin). No recall is linked to its devices.
FDA’s records also spell it “Dmp, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Dmp, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2012
2007high 4 (2010) · low 0 (2007)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dmp, Ltd.’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) Report