Espe GmbH & Co. Kg.

Espe GmbH & Co. Kg. holds 17 FDA 510(k) medical device clearances, first cleared 1995, most recent 1998.

Top product codes for Espe GmbH & Co. Kg.

ELW — Dental7 devices
EBF — Dental5 devices
EMA — Dental3 devices
EBG — Dental1 device
KLE — Dental1 device

Recent clearances by Espe GmbH & Co. Kg.

K974231 — POSITION PENTA, POSITION PENTA QUICKCode ELW·1998-01-29
K973513 — SINFONY DENTIN, OPAQUE-DENTIN, ENAMEL, ENAMEL MODIFIER, TRANSPARENT OPAL,SINFONY MAGIC MODIFIERS, SINFONY OPAQUERCode EBF·1997-12-22
K973262 — KETAC-FIL APLICAP PLUSCode EMA·1997-11-17
K972892 — CAVIT-LCCode EBF·1997-10-02
K963735 — COJET SYSTEMCode EBF·1996-11-27
K963737 — HYCEM APLICAPCode EMA·1996-11-15
K962428 — EBS (ESPE BONDING SYSTEM)Code KLE·1996-09-12
K962440 — PERTAC II/PERTAC II APLITIPCode EBF·1996-09-11
K962442 — HYTAC APLITIP/HYTAC OSBCode EBF·1996-09-11
K960954 — KETAC-MOLAR APLICAPCode EMA·1996-05-16
K960547 — DIMENSION PENTA/DIMENSION GARANT L/POLYVINYL SILOXANE ADHESIVECode ELW·1996-03-15
K954192 — IMPREGUM PENTACode ELW·1995-12-01
K954180 — MICROGLISSCode ELW·1995-11-21
K952693 — RAMITEC PENTACode ELW·1995-08-18
K953374 — PERMADYNE GARANT 2:1Code ELW·1995-08-18
K953027 — PERMADYNE PENTA (HIGH & LOW VISCOSITY)Code ELW·1995-07-19
K950203 — PROTEMP(R) GARANTCode EBG·1995-02-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.