Unicare Biomedical, Inc. is one of 4896 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unicare Biomedical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Unicare Biomedical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.
Historical record: 7 cleared submissions from 2001 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Unicare Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Unicare Biomedical, Inc.
7 devices
Cleared
Nov 19, 2015
Cytoflex Tefguard Ti-Enforced Membrane
Dental
184d
Cleared
Nov 25, 2009
MODIFICATION TO UNIGRAFT
Dental
97d
Cleared
Mar 23, 2009
CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
Dental
70d
Cleared
Nov 12, 2008
BENACEL, MODELS C-001, C-002 AND C-005
General & Plastic Surgery
260d
Cleared
Aug 06, 2002
CYTOFLEX MESH
Dental
89d
Cleared
May 07, 2002
OSSIFORM
Dental
63d
Cleared
Oct 01, 2001
CYTOFLEX
Dental
83d