Medical Device Manufacturer · US , Laguna Hills , CA

Unicare Biomedical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2001

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Unicare Biomedical, Inc. Dental ✕

6 devices

1-6 of 6

Cleared Nov 19, 2015

Cytoflex Tefguard Ti-Enforced Membrane

Cleared Nov 25, 2009

MODIFICATION TO UNIGRAFT

Cleared Mar 23, 2009

CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090

Cleared Aug 06, 2002

Cleared May 07, 2002

Cleared Oct 01, 2001