The Straumann Co.
The Straumann Co. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 23, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K041070 | STRAUMANN TEMPORARY COPING | July 23, 2004 |
| K040646 | STRAUMANN GRANULES | May 3, 2004 |
| K040469 | THE STRAUMANN ORTHO IMPLANT SYSTEM | April 30, 2004 |
| K993862 | MODUS SAGITTAL SPLIT PLATE | December 29, 1999 |
| K962023 | PLASTIC PROTECTION HEALING CAPS | August 15, 1996 |
| K960634 | TITANIUM HEALING CAPS | June 18, 1996 |
| K955281 | ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES | March 15, 1996 |
| K955369 | MEMFIX | January 23, 1996 |
| K941393 | ITI ANGLED ABUTMENT | June 14, 1995 |
| K943720 | ITI TRANSVERSAL SCREWING SYSTEM | March 24, 1995 |
| K931993 | ITI DISTANCE SYSTEM | April 26, 1994 |
| K923872 | BONE MARROW BIOPSY SYSTEM | December 15, 1992 |
| K920928 | PRE-STERILIZED ITI DENTAL IMPLANTS | July 15, 1992 |
| K920768 | HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM | April 21, 1992 |