Dmg USA, Inc.
FDA 510(k) medical device clearances.
Top product codes for Dmg USA, Inc.
Recent clearances by Dmg USA, Inc.
- K171772 — Ecosite Bulk Fill
- K160443 — TempoCem Clear
- K130580 — RETRACTION PASTE
- K110759 — TEMPOCEM
- K102603 — SA FLOWABLE ADHESIVE
- K101710 — LUXATEMP ULTRA /STAR
- K100062 — INFILTRATION KIT
- K093338 — SELF ADHESIVE COMPOSITE LUTING CEMENT
- K093587 — DENTAL MERCURY
- K081493 — INFILTRATION KIT
- K080480 — NANOCOMPOSITE RESTORATIVE KIT
- K080479 — DENTAL CERAMIC
- K063444 — TOTAL ETCH BONDING AGENT
- K052800 — PROVISIONAL INLAY/ONLAY KIT
- K041960 — COMPOSITE/COMPOMER REPAIR KIT
- K033227 — LUXAFORM PLUS
- K023649 — VITIQUE SYSTEM
- K013674 — LUXATEMP/LUXATEMP SOLAR/INSTATEMP
- K013571 — MAGICFIL
- K013237 — STATUSBLUE
- K013236 — LUXABITE
- K013179 — LUXAGLAZE
- K012307 — LUXACORE/LUXACORE DUAL
- K012316 — PERMACEM / PERMACEM DUAL
- K011211 — FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW
- K002086 — PRIMAFLOW
- K000878 — HONIGUM
- K000951 — LUXAFORM
Data sourced from openFDA. This site is unofficial and independent of the FDA.