The Straumann Co.
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041070 | STRAUMANN TEMPORARY COPING | NHA | 2004-07-23 | View |
| 510(k) | K040646 | STRAUMANN GRANULES | LYC | 2004-05-03 | View |
| 510(k) | K040469 | THE STRAUMANN ORTHO IMPLANT SYSTEM | OAT | 2004-04-30 | View |
| 510(k) | K993862 | MODUS SAGITTAL SPLIT PLATE | JEY | 1999-12-29 | View |
| 510(k) | K962023 | PLASTIC PROTECTION HEALING CAPS | DZE | 1996-08-15 | View |
| 510(k) | K960634 | TITANIUM HEALING CAPS | DZE | 1996-06-18 | View |
| 510(k) | K955281 | ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES | DZE | 1996-03-15 | View |
| 510(k) | K955369 | MEMFIX | DZL | 1996-01-23 | View |
| 510(k) | K941393 | ITI ANGLED ABUTMENT | DZE | 1995-06-14 | View |
| 510(k) | K943720 | ITI TRANSVERSAL SCREWING SYSTEM | DZE | 1995-03-24 | View |
| 510(k) | K931993 | ITI DISTANCE SYSTEM | DZE | 1994-04-26 | View |
| 510(k) | K923872 | BONE MARROW BIOPSY SYSTEM | GDM | 1992-12-15 | View |
| 510(k) | K920928 | PRE-STERILIZED ITI DENTAL IMPLANTS | DZE | 1992-07-15 | View |
| 510(k) | K920768 | HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM | DZE | 1992-04-21 | View |
No matching devices.
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