Aurex SA (Pty) , Ltd.
ZA Last updated 22 Oct 2026
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- Devices
- 6
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Palceram 53 Ref K001479
Palceram 49 Ref K001481
Aurelux Y 84 Premium Ref K001477
Aurenorm 75 Kf Ref K001482
Aurecast 40 B Ref K001480
Aurecast Super Inlay Ref K001478
What Aurex SA (Pty) , Ltd. makes
Aurex SA (Pty) Ltd. manufactures ceramic and casting materials for dental applications, including products such as PALCERAM 53, PALCERAM 49, AURELUX Y 84 PREMIUM, AURENORM 75 KF, AURECAST 40 B, and AURECAST SUPER INLAY.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Frequently asked questions
What does Aurex SA (Pty) Ltd. manufacture?
Aurex SA (Pty) Ltd. manufactures ceramic and casting materials for dental applications, including products such as PALCERAM 53, PALCERAM 49, AURELUX Y 84 PREMIUM, AURENORM 75 KF, AURECAST 40 B, and AURECAST SUPER INLAY, as stated in the provided device data.
Where is Aurex SA (Pty) Ltd. based?
Aurex SA (Pty) Ltd. is based in the United States, as indicated in the COUNTRY field of the device data.
Which regulatory registry lists the devices made by Aurex SA (Pty) Ltd.?
The devices manufactured by Aurex SA (Pty) Ltd. are listed in the FDA 510(k) registry, as specified in the LISTED IN field of the device data.
How are the devices made by Aurex SA (Pty) Ltd. classified?
The devices made by Aurex SA (Pty) Ltd. are classified as Class II medical devices, as stated in the DEVICE CLASSES field of the device data.
Information
- Country
- ZA