FDA 510(k) Applications Submitted by UNICARE BIOMEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090083 01/12/2009 CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090 UNICARE BIOMEDICAL, INC.
K080532 02/26/2008 BENACEL, MODELS C-001, C-002 AND C-005 UNICARE BIOMEDICAL, INC.
K020720 03/05/2002 OSSIFORM UNICARE BIOMEDICAL, INC.
K021511 05/09/2002 CYTOFLEX MESH UNICARE BIOMEDICAL, INC.
K151344 05/19/2015 Cytoflex Tefguard Ti-Enforced Membrane Unicare Biomedical, Inc.
K012144 07/10/2001 CYTOFLEX UNICARE BIOMEDICAL, INC.
K092567 08/20/2009 MODIFICATION TO UNIGRAFT UNICARE BIOMEDICAL, INC.


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