Tei Biosciences, Inc. is one of 4732 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tei Biosciences, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Tei Biosciences, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Boston, US.
Historical record: 16 cleared submissions from 2002 to 2017.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tei Biosciences, Inc.
16 devices
Cleared
Feb 16, 2017
SurgiMend MP Collagen Matrix for Soft Tissue Reconstruction
General & Plastic Surgery
115d
Cleared
Feb 22, 2016
PriMatrix Dermal Repair Scaffold
General & Plastic Surgery
61d
Cleared
Aug 05, 2013
PRIMATRIX DERMAL REPAIR SCAFFOLD
General & Plastic Surgery
91d
Cleared
Dec 10, 2010
PRIMATRIX AG ANTIMICROBIAL DERMAL DERMAL REPAIR SCAFFOLD
General & Plastic Surgery
316d
Cleared
Feb 04, 2009
SURGIMEND
General & Plastic Surgery
37d
Cleared
Dec 12, 2008
PRIMATRIX DERMAL REPAIR SCAFFOLD
General & Plastic Surgery
22d
Cleared
Aug 06, 2007
ORTHOMEND SOFT TISSUE MATRIX
General & Plastic Surgery
35d
Cleared
Jun 29, 2006
PRIMATRIX DERMAL REPAIR SCAFFOLD
General & Plastic Surgery
38d
Cleared
May 17, 2006
COSMATRIX
General & Plastic Surgery
51d
Cleared
May 17, 2006
XENFORM SOFT TISSUE REPAIR MATRIX
General & Plastic Surgery
37d
Cleared
May 15, 2006
TISSUEMEND SOFT TISSUE REPAIR MATRIX
General & Plastic Surgery
35d
Cleared
Aug 11, 2005
ORTHOMEND
General & Plastic Surgery
42d