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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 4-317
Standard
ISO  8325 Third edition 2023-03
Dentistry - Test methods for rotary instruments
Scope/Abstract
This document specifies general test methods for rotary instruments used in dentistry. These test methods are used for measuring the dimensional characteristics, neck strength and surface roughness of rotary instruments, such as burs, cutters, polishers, grinding instruments and rotary instruments used for oral surgery such as drills and countersinks.

Specific tests are specified in the respective instrument standards, if available.

This document does not specify test methods for materials used for rotary instruments.

NOTE For materials used for rotary instruments, see ISO 21850-1 and respective instrument standards.

This document is not applicable to endodontic instruments. For endodontic instruments, see ISO 3630-1.
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FDA recognition of ISO 8325 Second edition 2004-09 [Rec# 4-244] will be superseded by recognition of ISO 8325 Third edition 2023-03 [Rec# 4-317]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 4-244] until December 21, 2025. After this transition period, declarations of conformity to [Rec# 4-244] will not be accepted.
Public Law, CFR Citation(s) and Procode(s)*
Regulation Number Device Name Device Class Product Code
§872.3240 Bur, Dental Class 1 EJL
§872.3240 Bur, Diamond Coated, Reprocessed Class 1 NME
§872.4120 Saw, Bone, Ac-Powered Class 2 DZH
§872.4120 Drill, Bone, Powered Class 2 DZI
§872.4120 Driver, Wire, And Bone Drill, Manual Class 2 DZJ
§872.4120 Handpiece, Rotary Bone Cutting Class 2 KMW
§872.4120 Dental Stereotaxic Instrument Class 2 PLV
§872.4200 Controller, Foot, Handpiece And Cord Class 1 EBW
§872.4200 Handpiece, Belt And/Or Gear Driven, Dental Class 1 EFA
§872.4200 Handpiece, Air-Powered, Dental Class 1 EFB
§872.4200 Handpiece, Contra- And Right-Angle Attachment, Dental Class 1 EGS
§872.4200 Handpiece, Direct Drive, Ac-Powered Class 1 EKX
§872.4200 Handpiece, Water-Powered Class 1 EKY
§872.4200 Handpiece, Air-Powered, Root Canal Irrigation Class 1 NYL
§872.4535 Instrument, Diamond, Dental Class 1 DZP
§872.4535 Instrument, Diamond, Dental, Reprocessed Class 1 NLD
§872.6640 Unit, Operative Dental Class 1 EIA
Relevant FDA Guidance and/or Supportive Publications*
1. Guidance for Industry and FDA Staff: Dental Handpieces - Premarket Notification [510(k)] Submissions, issued May 2007.

2. Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling Guidance for Industry and Food and Drug Administration Staff, issued March 2015.

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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