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Straumann USA, LLC

FDA registration
Straumann USA, LLC·2 products·🇺🇸 United States

BLT TAP, 4.1, L25MM, SST/TAN

FDA Adverse Event
Injury ·INSTITUT STRAUMANN AG·Product code NDP·May 12, 2021

Straumann Palatal Implant , 04.1 L 4.2 mm, Article Number: 042.335S, Straumann USA., LLC, Andover, Massachusetts, 01810-1008

FDA Recall
Terminated ·Straumann USA LLC·Product code OAT·September 28, 2007

Straumann Palatal Implant , 4.8 L 4.2 mm, Article Number: 042.336S, Straumann USA., LLC, Andover, Massachusetts, 01810-1008

FDA Recall
Terminated ·Straumann USA LLC·Product code OAT·September 28, 2007

BLT Ø2.9MM SC, SLACTIVE® 12MM, RXD, LOXI

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 23, 2018

BLT Ø2.9MM SC, SLACTIVE® 12MM, RXD, LOXI

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 18, 2018

BLT Ø2.9MM SC, SLACTIVE® 14MM, RXD, LOXI

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 29, 2018

BLT Ø2.9MM SC, SLACTIVE® 10MM, RXD, LOXI

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 29, 2018

BLT Ø2.9MM SC, SLACTIVE® 10MM, RXD, LOXI

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 23, 2018

STRAUMANN

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code NHA·April 11, 2011

CIM Ø4.1MM RD, ZLA 8MM, AH4MM, ZRO2

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 5, 2019

CIM Ø4.1MM RD, ZLA 10MM, AH5.5MM, ZRO2

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 5, 2019

CIM Ø4.1MM RD, ZLA 12MM, AH5.5MM, ZRO2

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 2, 2019

CIM Ø4.1MM RD, ZLA 10MM, AH5.5MM, ZRO2

FDA Adverse Event
Injury ·STRAUMANN USA, LLC·Product code DZE·October 5, 2019

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

FDA Recall
Open, Classified ·Straumann USA LLC·Product code NDP·January 6, 2026

Straumann T-Sleeve 2.8mm, height 6mm, guided Article Number: 034.055V46 Intended for use as a drilling guide to prepare a site for placement of a dental implant into the dental implant site.

FDA Recall
Terminated ·Straumann Manufacturing Inc.·Product code NDP·June 4, 2009

KeyPrint Soft- bottle, 32.5 oz (1kg). Resin for the fabrication of orthodontic and dental appliances such as mouthguards, nightguards, splints and repositioners. Model (Ref) #: 4220005

FDA Recall
Open, Classified ·Straumann USA LLC·Product code MQC·June 25, 2021

Straumann SCS Screwdriver, driver, for ratchet, short, L 21mm, stainless steel Article Number: 046.401. dental surgical instrument.

FDA Recall
Terminated ·Straumann USA LLC·Product code NDP·May 27, 2021

WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.

FDA Recall
Open, Classified ·Straumann USA LLC·Product code NHA·April 17, 2025

Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;

FDA Recall
Open, Classified ·Straumann USA LLC·Product code NHA·March 17, 2026