Hi Bond Non-Precious Ceramic Alloy
FDA 510(k) K992881 · Matech, Inc.
510(k) numberK992881
Submission
- Device name
- Hi Bond Non-Precious Ceramic Alloy
- Applicant
- Matech, Inc.
Sylmar, CA, US - Received
- August 26, 1999
- Decision date
- November 19, 1999
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Other 510(k)s with product code EJH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K123929 | Begopal+EJH · Abbreviated | Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO | 03/14/2013SE |
| K040180 | Continum VEJH · Traditional | Aalba Dent, Inc. | 03/04/2004SE |
| K040179 | ContinumEJH · Traditional | Aalba Dent, Inc. | 03/03/2004SE |
| K033356 | Verasoft EsEJH · Traditional | Aalba Dent, Inc. | 12/30/2003SE |
| K033045 | Dream Bond, Dreamcast Chrome, Dreamcast V, Dream Flexicast, Dream LithecastEJH · Traditional | American Green Dent. Mfg, Inc. | 12/23/2003SE |
| K032136 | Wirobond CEJH · Traditional | Bego U.S.A. | 09/04/2003SE |
| K031627 | Nano-TicrownEJH · Traditional | Nano-Write Corp. | 06/11/2003SE |
| K030632 | PD Casta-HEJH · Traditional | Mountain Medico, Inc. | 05/07/2003SE |
| K030416 | Ceracast-VEJH · Traditional | Mountain Medico, Inc. | 04/14/2003SE |
| K030161 | SuperbondEJH · Traditional | American Dent-All, Inc. | 03/17/2003SE |
More from American Dent-All, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K010069 | Durabond Non-Precious Ceramic AlloyEJH · Traditional | 02/15/2001SE |
| K993572 | Ceradium V Non-Precious Ceramic AlloyEJH · Traditional | 12/13/1999SE |
| K992705 | Ceradium Non-Precious Ceramic AlloyEJH · Traditional | 09/22/1999SE |
| K974894 | Kromatica Color Changing AlginateELW · Traditional | 02/12/1998SE |
| K925746 | ReplicaELW · Traditional | 01/21/1994SE |
Questions and answers
When was Hi Bond Non-Precious Ceramic Alloy cleared by the FDA?
Hi Bond Non-Precious Ceramic Alloy (K992881) received a 510(k) decision of Substantially Equivalent on November 19, 1999, 85 days after the submission was received.
What is the product code of K992881?
The FDA product code is EJH – Alloy, Metal, Base, a Class II (moderate risk) device regulated under 21 CFR 872.3710.