This page includes the latest FDA filings for Sintea Biotech Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
|---|---|---|
SINTEA BIOTECH, INC. | LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X | 2009-04-07 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH PLS MULTI-AXIAL SCREWS | 2008-07-18 |
SINTEA BIOTECH, INC. | X-VOID, SPIDER | 2008-06-06 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH DSC/ALF SPINAL SYSTEM, DSC.XX.T5.XX, ALF.XX.T5.XX | 2007-04-18 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH PLS MULTI-AXIAL SCREWS, MODEL PLS.XX.T5.X | 2006-03-10 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM WITH POLYAXIAL AND RECOVERY SCREWS, MODEL PLS.01.T5.X | 2004-12-17 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH ANTERIOR PLATE SYSTEM, MODEL ACP.XX.T5.X | 2004-09-16 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH SCHANZ SCREW, MODEL TFX.SS.XX.X | 2003-06-24 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X | 2002-12-10 |
SINTEA BIOTECH, INC. | SINTEA BIOTECH TRAUMAFIX SYSTEM, MODEL TFX.00.00.X | 2002-08-06 |
| NCAGE Code | 56GX0 | SINTEA BIOTECH INC |
| CAGE Code | 56GX0 | SINTEA BIOTECH INC |