ClearanceBrief
Company ยท US

Unicare Biomedical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2015. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LYCBone Grafting Material, Synthetic7
JEYPlate, Bone1
NPKBarrier, Synthetic, Intraoral1
OLROral Wound Dressing1
QSYHemostatic Wound Dressing Without Thrombin Or Other Biologics1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 19, 2015K151344Cytoflex Tefguard Ti-Enforced Membrane
Unicare Biomedical, Inc.
NPK
Nov 25, 2009K092567MODIFICATION TO UNIGRAFT
Unicare Biomedical, Inc.
LYC
Jul 24, 2009K090612BENACEL
Unicare Biomedical
OLR
Mar 23, 2009K090083CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
Unicare Biomedical, Inc.
LYC
Nov 12, 2008K080532BENACEL, MODELS C-001, C-002 AND C-005
Unicare Biomedical, Inc.
QSY
Aug 6, 2002K021511CYTOFLEX MESH
Unicare Biomedical, Inc.
JEY
May 7, 2002K020720OSSIFORM
Unicare Biomedical, Inc.
LYC
Oct 1, 2001K012144CYTOFLEX
Unicare Biomedical, Inc.
LYC
Jan 9, 2001K003457UNIGRAFT
Unicare Biomedical
LYC
Jan 27, 2000K993784UNIGRAFT
Unicare Biomedical
LYC
Oct 20, 1998K982699UNIGRAFE
Unicare Biomedical
LYC

Latest recalls

DateFirm and productCodeLinked 510(k)
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