Espe Dental AG
Espe Dental AG holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2001.
Top product codes for Espe Dental AG
Recent clearances by Espe Dental AG
- K011394 — LAVA FRAME, LAVA FRAME SHADE, LAVA CERAM
- K011154 — ELIPAR FREELIGHT
- K002793 — KETAC CEM U
- K002364 — PROTEMP H
- K001494 — MODIFICATION TO PROMPT L-POP
- K000595 — DIMENSION PENTA L
- K000588 — DIMENSION GARANT L, DIMENSION GARANT L QUICK
- K000591 — DIMENSION PENTA H, DIMENSION PENTA H QUICK
- K994192 — IMPREGUM PENTA M MONOSOFT
- K994193 — IMPREGUM PENTA DUOSOFT
- K994190 — IMPREGUM GARANT L DUOSOFT
- K994251 — KETAC-MOLAR QUICK
- K993566 — PROMPTFLOW
- K992909 — HYTAC
- K992966 — REFERENCE
- K992645 — SINFONY
- K992895 — IMPREGUM F
- K992897 — IMPREGUM PENTA
- K992048 — MODIFICATION OF PROMPT L-POP
- K991913 — PENTAMIX 2
- K991008 — DIMENSION BITE
- K990763 — VITRON M
- K991220 — VITRON H
- K991221 — VESTOGUM
- K990982 — CAVIT LC
- K984247 — ELIPAR TRILIGHT
- K984246 — PROMPT L-POP
- K984248 — PROCEM
- K983414 — EVERBOND
Data sourced from openFDA. This site is unofficial and independent of the FDA.