Herculite Ultra Flow 35389
Herculite Ultra Flow 35389 is a light-cured dental restorative composite resin (FDA Class II; FDA product code EBF, Material, Tooth Shade, Resin) made by Kerr Corporation, listed in FDA GUDID since 1 Aug 2016 (UDI-DI 00841396110597), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841396110597 | Date1 Aug 2016 | StatusListed |
Official records
- AccessGUDID record 00841396110597
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Herculite Ultra Flow
- Generic name
- Light-cured dental restorative composite resin
- Model / Ref / Catalog
- 35389
- Primary DI / UDI-DI
- 00841396110597
- FDA product code
- EBF
- GMDN term
- Light-cured dental restorative composite resin
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 1 Gram
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