The Straumann Co.
FDA 510(k) medical device clearances.
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.