The Straumann Co.
The Straumann Co. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2004.
Top product codes for The Straumann Co.
Recent clearances by The Straumann Co.
- K041070 — STRAUMANN TEMPORARY COPING
- K040646 — STRAUMANN GRANULES
- K040469 — THE STRAUMANN ORTHO IMPLANT SYSTEM
- K993862 — MODUS SAGITTAL SPLIT PLATE
- K962023 — PLASTIC PROTECTION HEALING CAPS
- K960634 — TITANIUM HEALING CAPS
- K955281 — ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
- K955369 — MEMFIX
- K941393 — ITI ANGLED ABUTMENT
- K943720 — ITI TRANSVERSAL SCREWING SYSTEM
- K931993 — ITI DISTANCE SYSTEM
- K923872 — BONE MARROW BIOPSY SYSTEM
- K920928 — PRE-STERILIZED ITI DENTAL IMPLANTS
- K920768 — HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM
Data sourced from openFDA. This site is unofficial and independent of the FDA.