Henry Schein 1000261
Henry Schein 1000261 is a dental polishing cup (FDA Class I; FDA product code EFB, Handpiece, air-powered, dental) made by Henry Schein, Inc., cleared under FDA 510(k) K073652 on 20 Mar 2008 and listed in FDA GUDID since 26 Nov 2019 (UDI-DI 00304040057742), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00304040057742 | Date26 Nov 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK073652 | Date20 Mar 2008 | StatusActive |
Official records
- AccessGUDID record 00304040057742
- FDA 510(k) database K073652
Across registries
- FDA 510(k) K073652 decided 20 Mar 2008 Active
- FDA GUDID UDI-DI 00304040057742 listed 26 Nov 2019 Listed
Timeline
- Cleared FDA 510(k) K073652
- Listed FDA GUDID 00304040057742
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Henry Schein
- Generic name
- Dental polishing cup, reusable
- Model / Ref / Catalog
- 1000261
- Primary DI / UDI-DI
- 00304040057742
- 510(k) Number
- FDA product code
- EFB
- GMDN term
- Dental polishing cup, reusable
- Device class
- Class I
- Regulation number
- 872.4200
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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