Nanoceram- Bright
by Dmp, Ltd. 510(k)
Active
510(k) K102257
Overview
The NANOCERAM- BRIGHT is a dental device classified under product code EBF. It is designed for use in dental applications, as indicated by its advisory committee designation.
This device is manufactured by Dmp, Ltd. and received FDA 510K clearance on November 19, 2010, with K number K102257. The device is supplied as a single-use product and should be stored according to the manufacturer's instructions.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK102257 | Date19 Nov 2010 | 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- Withdrawn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
- EBF
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.3690
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent
Other devices from Dmp, Inc.
Questions
What is the NANOCERAM-BRIGHT device used for?
The NANOCERAM-BRIGHT is a dental device classified under product code EBF, specifically designed for dental applications as indicated by its advisory committee designation.
Is the NANOCERAM-BIRT device reusable or single-use?
The NANOCERAM-BRIGHT is supplied as a single-use product and should be used only once according to the manufacturer's instructions.
What regulatory clearance does the NANOCERAM-BRIGHT have?
The NANOCERAM-BRIGHT received FDA 510K clearance on November 19, 2010, with K number K102257, and was determined to be substantially equivalent.
How should the NANOCERAM-BRIGHT be stored?
The NANOCERAM-BRIGHT should be stored according to the manufacturer's instructions, though specific storage conditions are not detailed in the provided information.