Omnichroma 10132
by Tokuyama Dental Corporation
Omnichroma 10132 is a Class II device made by Tokuyama Dental Corporation, cleared under FDA 510(k) K173275 on 27 Feb 2018 and listed in FDA GUDID since 15 May 2018 (UDI-DI 04548190101320), active as of 23 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 | Number04548190101320 | Date15 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173275 | Date27 Feb 2018 | StatusActive |
Official records
- AccessGUDID record 04548190101320
- FDA 510(k) database K173275
Across registries
- FDA 510(k) K173275 decided 27 Feb 2018 Active
- FDA GUDID UDI-DI 04548190101320 listed 15 May 2018 Listed
Timeline
- Cleared FDA 510(k) K173275
- Listed FDA GUDID 04548190101320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Omnichroma
- Generic name
- Dental composite resin
- Model / reference
- 10132
- Primary DI / UDI-DI
- 04548190101320
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Dental composite resin
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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