Medical Device Manufacturer · US , Laguna Hills , CA

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

7 submissions · 7 cleared · Since 2001

Recent clearances: Cytoflex Tefguard Ti-Enforced Membrane, MODIFICATION TO UNIGRAFT, CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Unicare Biomedical, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Nov 12, 2008

BENACEL, MODELS C-001, C-002 AND C-005

General & Plastic Surgery · 260d