Medical Device Manufacturer · US , Cambridge , MA

The Straumann Co.

14 submissions · 14 cleared · Since 1992
14
Total
14
Cleared
0
Denied

The Straumann Co. has 14 FDA 510(k) cleared dental devices. Based in Cambridge, US.

Historical record: 14 cleared submissions from 1992 to 2004.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

14 devices
1–12 of 14
STRAUMANN TEMPORARY COPING
K041070 · NHA Abutment, Implant, Dental, Endosseous · Dental
Jul 2004 88d
STRAUMANN GRANULES
K040646 · LYC Bone Grafting Material, Synthetic · Dental
May 2004 53d
THE STRAUMANN ORTHO IMPLANT SYSTEM
K040469 · OAT Implant, Endosseous, Orthodontic · Dental
Apr 2004 66d
MODUS SAGITTAL SPLIT PLATE
K993862 · JEY Plate, Bone · Dental
Dec 1999 44d
PLASTIC PROTECTION HEALING CAPS
K962023 · DZE Implant, Endosseous, Root-form · Dental
Aug 1996 84d
TITANIUM HEALING CAPS
K960634 · DZE Implant, Endosseous, Root-form · Dental
Jun 1996 125d
ENDOSSEOUS DENTAL IMPLANT & ACCESSORIES
K955281 · DZE Implant, Endosseous, Root-form · Dental
Mar 1996 120d
MEMFIX
K955369 · DZL Screw, Fixation, Intraosseous · Dental
Jan 1996 60d
ITI ANGLED ABUTMENT
K941393 · DZE Implant, Endosseous, Root-form · Dental
Jun 1995 449d
ITI TRANSVERSAL SCREWING SYSTEM
K943720 · DZE Implant, Endosseous, Root-form · Dental
Mar 1995 235d
ITI DISTANCE SYSTEM
K931993 · DZE Implant, Endosseous, Root-form · Dental
Apr 1994 368d
BONE MARROW BIOPSY SYSTEM
K923872 · GDM Needle, Aspiration And Injection, Reusable · General & Plastic Surgery
Dec 1992 134d
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