Master-Dent 18-124
Master-Dent 18-124 is a device made by Dentonics, Inc., cleared under FDA 510(k) K823510 on 28 Dec 1982 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00816526021456), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816526021456 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK823510 | Date28 Dec 1982 | StatusActive |
Official records
- AccessGUDID record 00816526021456
- FDA 510(k) database K823510
Across registries
- FDA 510(k) K823510 decided 28 Dec 1982 Active
- FDA GUDID UDI-DI 00816526021456 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K823510
- Listed FDA GUDID 00816526021456
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Master-Dent
- Generic name
- Dental tooth-etching solution
- Model / reference
- 18-124
- Description
- Blue Gel Etch, 4 x 3 ml syringes w/ 20 blue luer lock needle tips
- Primary DI / UDI-DI
- 00816526021456
- 510(k) Number
- GMDN term
- Dental tooth-etching solution
- GUDID distribution status
- In Commercial Distribution