Medical Device Manufacturer · DE , Bavaria D-82228 Seefeld

Espe Dental AG - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1998

Recent clearances: LAVA FRAME, LAVA FRAME SHADE, LAVA CERAM, ELIPAR FREELIGHT, KETAC CEM U

29

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Espe Dental AG Dental ✕

29 devices

1-12 of 29

Cleared Jun 29, 2001

LAVA FRAME, LAVA FRAME SHADE, LAVA CERAM

Cleared May 16, 2001

ELIPAR FREELIGHT

Cleared Sep 26, 2000

Cleared Aug 10, 2000

Cleared Jul 07, 2000

MODIFICATION TO PROMPT L-POP

Cleared Apr 05, 2000

DIMENSION PENTA L

Cleared Mar 30, 2000

DIMENSION GARANT L, DIMENSION GARANT L QUICK

Cleared Mar 30, 2000

DIMENSION PENTA H, DIMENSION PENTA H QUICK

Cleared Jan 28, 2000

IMPREGUM PENTA M MONOSOFT

Cleared Jan 28, 2000

IMPREGUM PENTA DUOSOFT

Cleared Jan 27, 2000

IMPREGUM GARANT L DUOSOFT

Cleared Jan 03, 2000

KETAC-MOLAR QUICK