Medical Device Manufacturer · DE , Bavaria D-82228 Seefeld

Espe Dental AG - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1998

Total

Cleared

Denied

Espe Dental AG has 29 FDA 510(k) cleared dental devices. Based in Bavaria D-82228 Seefeld, DE.

Historical record: 29 cleared submissions from 1998 to 2001.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Espe Dental AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Espe Dental AG

29 devices

1-12 of 29

Cleared Jun 29, 2001

LAVA FRAME, LAVA FRAME SHADE, LAVA CERAM

MODIFICATION TO PROMPT L-POP

DIMENSION GARANT L, DIMENSION GARANT L QUICK

K000588 · ELW

Dental · 37d

Cleared Mar 30, 2000

DIMENSION PENTA H, DIMENSION PENTA H QUICK

K000591 · ELW

Dental · 37d

Cleared Jan 28, 2000

IMPREGUM PENTA M MONOSOFT

K994192 · ELW

Dental · 46d

Cleared Jan 28, 2000

IMPREGUM PENTA DUOSOFT

K994193 · ELW

Dental · 46d

Cleared Jan 27, 2000

IMPREGUM GARANT L DUOSOFT

Espe Dental AG - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Espe Dental AG

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