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U.S. Department of Health and Human Services

Recognized Consensus Standards: Medical Devices

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Part B: Supplementary Information Sheet (SIS)
FR Recognition List Number 061 Date of Entry 12/18/2023 
FR Recognition Number 4-313
Standard
ISO  27020 Second edition 2019-06
Dentistry - Brackets and tubes for use in orthodontics
Identical Adoption
ANSI ADA Standard No.100-2020
Orthodontic Brackets and Tubes
Scope/Abstract
This document specifies requirements and test methods to compare the functional dimensions of orthodontic brackets and tubes and their chemical ion release, as well as packaging and labelling information.

This document is applicable to brackets and tubes for use in fixed orthodontic appliances.

This document does not specify specific qualitative and quantitative requirements for freedom from biological hazards; which are covered in ISO 10993-1 and ISO 7405.
Extent of Recognition
Complete standard
Rationale for Recognition
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.
Transition Period
FDA recognition of ISO 27020 First edition 2010-12 [Rec# 4-218] will be superseded by recognition of ISO 27020 Second edition 2019-06 [Rec# 4-313]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 4-218] until December 21, 2025. After this transition period, declarations of conformity to [Rec# 4-218] will not be accepted.
Public Law, CFR Citation(s) and Procode(s)*
Regulation Number Device Name Device Class Product Code
§872.5410 Tube, Orthodontic Class 1 DZD
§872.5410 Bracket, Metal, Orthodontic Class 1 EJF
§872.5410 Bracket, Metal, Orthodontic, Reprocessed Class 1 NQS
§872.5470 Bracket, Plastic, Orthodontic Class 2 DYW
§872.5470 Bracket, Ceramic, Orthodontic Class 2 NJM
§872.5470 Bracket, Plastic, Orthodontic, Reprocessed Class 2 NLC
Relevant FDA Guidance and/or Supportive Publications*
Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices - Guidance for Industry and Food and Drug Administration Staff, issued September 2018.
FDA Technical Contacts
 Lauren Giles
  FDA/OC/CDRH/OPEQ/OHTI/DHTIB/
  301-796-9552
  lauren.giles@fda.hhs.gov
 Bobak Shirmohammadi
  FDA/OC/CDRH/OPEQ/OHTI/DHTIB/
  301-796-3639
  Bobak.Shirmohammadi@fda.hhs.gov
Standards Development Organization
ISO International Organization for Standardization https://www.iso.org/
FDA Specialty Task Group (STG)
Dental/ENT
*These are provided as examples and others may be applicable.
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