Medical Device Manufacturer · DE , Seefeld

Espe GmbH & Co. Kg. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1995

Total

Cleared

Denied

Espe GmbH & Co. Kg. has 17 FDA 510(k) cleared dental devices. Based in Seefeld, DE.

Historical record: 17 cleared submissions from 1995 to 1998.

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

Espe GmbH & Co. Kg. 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 GmbH & Co. Kg.

17 devices

1-12 of 17

Cleared Jan 29, 1998

POSITION PENTA, POSITION PENTA QUICK

K974231 · ELW

Dental · 78d

Cleared Dec 22, 1997

SINFONY DENTIN, OPAQUE-DENTIN, ENAMEL, ENAMEL MODIFIER, TRANSPARENT...

K973513 · EBF

Dental · 96d

Cleared Nov 17, 1997

KETAC-FIL APLICAP PLUS

EBS (ESPE BONDING SYSTEM)

K962428 · KLE

Dental · 80d

Cleared Sep 11, 1996

PERTAC II/PERTAC II APLITIP

K962440 · EBF

Dental · 79d

Cleared Sep 11, 1996

HYTAC APLITIP/HYTAC OSB

DIMENSION PENTA/DIMENSION GARANT L/POLYVINYL SILOXANE ADHESIVE

Espe GmbH & Co. Kg. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Espe GmbH & Co. Kg.

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