Straumann USA, LLC is one of 14046 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Straumann USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: Straumann® Anatomic Healing Abutments XC (AHA), Straumann Surgical Cassettes, Straumann 4 mm Short Implants
24
Total
24
Cleared
0
Denied
Straumann USA, LLC has 24 FDA 510(k) cleared dental devices. Based in Andover, US.
Latest FDA clearance: Nov 2024. Active since 2012.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Heyer Regulatory Solutions, LLC and Straumann USA, Lls.
FDA 510(k) Regulatory Record - Straumann USA, LLC
24 devices
Cleared
Nov 11, 2024
Straumann® Anatomic Healing Abutments XC (AHA)
Dental
161d
Cleared
Jul 29, 2021
Straumann Surgical Cassettes
General Hospital
218d
Cleared
Feb 08, 2021
Straumann 4 mm Short Implants
Dental
131d
Cleared
Apr 06, 2020
Straumann Screw-Retained Abutments
Dental
216d
Cleared
Jun 17, 2019
MRI Compatibility for Existing Straumann Dental Implant Systems
Dental
94d
Cleared
Jan 19, 2018
Straumann Dental Implant System
Dental
218d
Cleared
Mar 08, 2017
BLT 02.9mm SC, SLA or SLActive, RXD, Loxim, SC Closure Cap and Healing...
Dental
142d
Cleared
Mar 04, 2016
Straumann RN Gold Abutment for Bridge
Dental
266d
Cleared
Sep 16, 2015
Straumann CARES Titanium Alloy (TAN) Abutment
Dental
166d
Cleared
Sep 11, 2015
Straumann Variobase for CEREC
Dental
116d
Cleared
Aug 10, 2015
Straumann Screw-Retained Abutment
Dental
136d
Cleared
Aug 10, 2015
NC Straumann Screw Retained Abutments
Dental
91d