Alflbl
by Flexmedics
Alflbl is a Class II device made by Flexmedics, listed in FDA GUDID since 27 May 2020 (UDI-DI 10195291007542), 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 | Number10195291007542 | Date27 May 2020 | StatusListed |
Official records
- AccessGUDID record 10195291007542
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Alginate dental impression material
- Model / reference
- ALFLBL
- Primary DI / UDI-DI
- 10195291007542
- FDA product code
- ELW
- GMDN term
- Alginate dental impression material
- Device class
- Class II
- Regulation number
- 872.3660
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code ELW (Material, Impression).
- TORPICALGIN by Zhermack S.P.A.
- Mousse, Polyvinyl Siloxane Impression Material by PARKELL, INC.
- Hydrocolor 5 by Cascades Device Consulting Associates
- IMPRESSION COMPOUND by Spofadental
- New Light-Curing Impression Material by Dentsply Intl.
- COLORISE by Zhermack S.P.A.
- Deguflex Monophase by Degussa AG
- Rhodia Dental Putty Impression Material by Rhodia, Inc.
- Hyunjae Dental Impression Materials by Hyunjae Corp.
- Aquasil Ultra Monophase/Heavy/LV Smart Wetting Impression Material by Dentsply Intl.