Treo 4224-671
Treo 4224-671 is a Class II device made by Benco Dental Supply Co., cleared under FDA 510(k) K941327 on 22 Dec 1994 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00366975000699), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00366975000699 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK941327 | Date22 Dec 1994 | StatusActive |
Official records
- AccessGUDID record 00366975000699
- FDA 510(k) database K941327
Across registries
- FDA 510(k) K941327 decided 22 Dec 1994 Active
- FDA GUDID UDI-DI 00366975000699 listed 23 Sep 2016 Listed
Recalls
-
- Ongoing Z-1791-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Timeline
- Cleared FDA 510(k) K941327
- Listed FDA GUDID 00366975000699
- Recall initiated FDA recalls Z-1791-2022
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Treo
- Generic name
- Sterilization packaging, single-use
- Model / reference
- 4224-671
- Primary DI / UDI-DI
- 00366975000699
- 510(k) Number
- FDA product code
- KCT
- GMDN term
- Sterilization packaging, single-use
- Device class
- Class II
- Regulation number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
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