Tei Biosciences, Inc.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162965 | SurgiMend MP Collagen Matrix for Soft Tissue Reconstruction | FTM | 2017-02-16 | View |
| 510(k) | K153690 | PriMatrix Dermal Repair Scaffold | KGN | 2016-02-22 | View |
| 510(k) | K131286 | PRIMATRIX DERMAL REPAIR SCAFFOLD | KGN | 2013-08-05 | View |
| 510(k) | K100261 | PRIMATRIX AG ANTIMICROBIAL DERMAL DERMAL REPAIR SCAFFOLD | FRO | 2010-12-10 | View |
| 510(k) | K083898 | SURGIMEND | FTM | 2009-02-04 | View |
| 510(k) | K083440 | PRIMATRIX DERMAL REPAIR SCAFFOLD | KGN | 2008-12-12 | View |
| 510(k) | K071807 | ORTHOMEND SOFT TISSUE MATRIX | FTM | 2007-08-06 | View |
| 510(k) | K061407 | PRIMATRIX DERMAL REPAIR SCAFFOLD | KGN | 2006-06-29 | View |
| 510(k) | K060984 | XENFORM SOFT TISSUE REPAIR MATRIX | FTM | 2006-05-17 | View |
| 510(k) | K060829 | COSMATRIX | FTM | 2006-05-17 | View |
| 510(k) | K060989 | TISSUEMEND SOFT TISSUE REPAIR MATRIX | FTM | 2006-05-15 | View |
| 510(k) | K051766 | ORTHOMEND | FTL | 2005-08-11 | View |
| 510(k) | K051190 | XENFORM SOFT TISSUE REPAIR MATRIX | PAJ | 2005-06-10 | View |
| 510(k) | K023778 | DRESSSKIN | KGN | 2003-09-29 | View |
| 510(k) | K031188 | ORTHOMEND | FTL | 2003-06-27 | View |
| 510(k) | K020455 | TISSUEMEND SOFT TISSUE REPAIR MATRIX | FTM | 2002-04-03 | View |
No matching devices.
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