Mach Brackets Bright Brackets
FDA 510(k) K120471 · World Bio Tech Co., Ltd.
510(k) numberK120471
Submission
- Device name
- Mach Brackets Bright Brackets
- Applicant
- World Bio Tech Co., Ltd.
Pittsburgh, PA, US - Received
- February 16, 2012
- Decision date
- June 4, 2012
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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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|---|---|---|---|
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| K232011 | CleoNJM · Traditional | American Orthodontics | 07/07/2023SE |
| K231635 | A-Line AdvancedNJM · Traditional | Biocetec Co., Ltd. | 06/06/2023SE |
| K230225 | DynaFlex Clear Brackets & ButtonsNJM · Traditional | Dyna Flex | 06/05/2023SE |
| K222847 | Ceramic Brackets OrthometricNJM · Traditional | Orthometric - Industria E Comercio DE Produtos… | 05/04/2023SE |
| K222764 | LightForce Orthodontic SystemNJM · Special | Lightforce Orthodontics | 09/14/2022SE |
| K220689 | Vatech ClismileNJM · Traditional | Rayence Co., Ltd. | 05/06/2022SE |
| K201410 | VENUS Bracket, ROSE BracketNJM · Traditional | Gni Co., Ltd. | 03/12/2021SE |
| K201038 | Luce Ceramic BracketNJM · Traditional | Luce Castle Co., Ltd. | 10/09/2020SE |
| K200148 | LightForce Orthodontic System (LFO System)NJM · Traditional | Lightforce Orthodontics | 02/21/2020SE |
More from Lightforce Orthodontics
| 510(k) | Device | Decision |
|---|---|---|
| K152167 | BIJOU Orthodontic Ceramic BracketNJM · Traditional | 05/27/2016SE |
Questions and answers
When was Mach Brackets Bright Brackets cleared by the FDA?
Mach Brackets Bright Brackets (K120471) received a 510(k) decision of Substantially Equivalent on June 4, 2012, 109 days after the submission was received.
What is the product code of K120471?
The FDA product code is NJM – Bracket, Ceramic, Orthodontic, a Class II (moderate risk) device regulated under 21 CFR 872.5470.