Truklear Bracket

FDA 510(k) K141104 · Ajw Technology Consultants, Inc.

Substantially Equivalent

510(k) numberK141104

Submission

Device name
Truklear Bracket
Applicant
Ajw Technology Consultants, Inc.
Apollo Beach, FL, US
Received
April 29, 2014
Decision date
June 25, 2014
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NJM – Bracket, Ceramic, Orthodontic
Device class
Class II (moderate risk)
Regulation
21 CFR 872.5470
Specialty
Dental

An orthodontic ceramic bracket is a device composed of ceramic, which is intended to be bonded to a tooth, upon which an orthodontic wire is used to move the tooth to a new position.

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Questions and answers

When was Truklear Bracket cleared by the FDA?

Truklear Bracket (K141104) received a 510(k) decision of Substantially Equivalent on June 25, 2014, 57 days after the submission was received.

What is the product code of K141104?

The FDA product code is NJM – Bracket, Ceramic, Orthodontic, a Class II (moderate risk) device regulated under 21 CFR 872.5470.