Medical Device Manufacturer · US , Cambridge , MA

The Straumann Co. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1992

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Straumann Co. Dental ✕

13 devices

1-13 of 13

Cleared Jul 23, 2004

STRAUMANN TEMPORARY COPING

Cleared May 03, 2004

STRAUMANN GRANULES

Cleared Apr 30, 2004

THE STRAUMANN ORTHO IMPLANT SYSTEM

Cleared Dec 29, 1999

MODUS SAGITTAL SPLIT PLATE

Cleared Aug 15, 1996

PLASTIC PROTECTION HEALING CAPS

Cleared Jun 18, 1996

TITANIUM HEALING CAPS

Cleared Mar 15, 1996

ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES

Cleared Jan 23, 1996

Cleared Jun 14, 1995

ITI ANGLED ABUTMENT

Cleared Mar 24, 1995

ITI TRANSVERSAL SCREWING SYSTEM

Cleared Apr 26, 1994

ITI DISTANCE SYSTEM

Cleared Jul 15, 1992

PRE-STERILIZED ITI DENTAL IMPLANTS

Cleared Apr 21, 1992

HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM