Dentatus USA , Ltd.

Dentatus USA , Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 1996, most recent 2004.

Top product codes for Dentatus USA , Ltd.

Recent clearances by Dentatus USA , Ltd.

K042931 — TUF LINK SILICONE RELINERCode EBI·2004-12-08
K031793 — DENTATUS OSCIOMATCode DZH·2003-11-13
K980620 — DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEMCode DZE·1998-05-15
K961704 — MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEMCode ELS·1996-07-26

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