Tissue Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002071 | SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLES | FTL | 2000-07-24 | View |
| 510(k) | K000849 | SOFTFORM FACIAL IMPLANT | FTL | 2000-05-19 | View |
| 510(k) | K982475 | SOFT TISSUE AUGMENTATION YUBE WITH INSERTION TOOL | FTL | 1998-09-22 | View |
| 510(k) | K973462 | SOFTFORM FACIAL IMPLANT | FTL | 1997-11-24 | View |
| 510(k) | K970804 | TRU-PULSE CO2 SURGICAL LASER | GEX | 1997-06-03 | View |
| 510(k) | K963683 | TRU-PULSE LASER (MODIFIED) | GEX | 1997-02-12 | View |
| 510(k) | K962496 | SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.) | FTL | 1996-09-03 | View |
| 510(k) | K960481 | SOFT TISSUE AUGMENTATION TUBE | FTL | 1996-04-01 | View |
| 510(k) | K952049 | TRU-PULSE PULSED CO2 SURGICAL LASER SYSTEM | GEX | 1995-07-21 | View |
No matching devices.
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