Dmg USA, Inc.
Dmg USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2018.
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.