Aurelux Bio Y85PF
by Aurex Precious Metal Industries (Pty)Ltd 510(k)
Active
510(k) K972949
Overview
The Aurelux Bio Y85PF is a gold-based noble metal alloy used in dental applications. It is classified as a class 2 dental device.
This device is subject to FDA 510(k) clearance under regulation number 872.3060. It is manufactured by Aurex Precious Metal Industries (Pty)Ltd.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK972949 | Date18 Sep 1997 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- EJT
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.3060
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent
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Questions
What is the Aurelux Bio Y85PF used for?
The Aurelux Bio Y85PF is a gold-based noble metal alloy specifically formulated for use in dental applications.
What is the regulatory status of this dental alloy?
This device is classified as a class 2 dental device and has received FDA 510(k) clearance under regulation number 872.3060.
Who is the manufacturer of the Aurelux Bio Y85PF?
The device is manufactured by Aurex Precious Metal Industries (Pty)Ltd, located in Edenvale, South Africa.