Clarity™ ADVANCED 006-151
Ref 006-151
Clarity™ ADVANCED 006-151 is a device classified as Class IIa in the EU and Class II in the US made by 3M Unitek Corporation, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI B-00652221223029) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00652221223029), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00652221223029 00652221223029 | Date30 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00652221223029 | Date24 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-00652221223029
- AccessGUDID record 00652221223029
Across registries
- EUDAMED Basic UDI-DI B-00652221223029 registered 30 Oct 2026 Active
- FDA GUDID UDI-DI 00652221223029 listed 24 Sep 2016 Listed
Timeline
- Listed FDA GUDID 00652221223029
- Registered EUDAMED B-00652221223029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- 3M™ Clarity™ EUDAMEDClarity™ ADVANCED GUDID
- Generic name
- Orthodontic bracket, ceramic
- Device name
- 3M™ Clarity™ Advanced Ceramic Brackets - 006-151
- Model / Ref / Catalog
- 006-151
- Primary DI / UDI-DI
- 00652221223029
- Basic UDI-DI
- B-00652221223029
- FDA product code
- NJM
- EMDN code
- Q010403 Orthodontic brackets and buttons
- GMDN term
- Orthodontic bracket, ceramic
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 872.5470
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
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