Bosworth Superbite 0921817
Bosworth Superbite 0921817 is a Class II device made by Harry J. Bosworth Co., listed in FDA GUDID since 15 Sep 2016 (UDI-DI H66809218171), 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 | NumberH66809218171 | Date15 Sep 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bosworth Superbite
- Generic name
- Composite dental impression material
- Model / Ref / Catalog
- 0921817
- Primary DI / UDI-DI
- H66809218171
- FDA product code
- ELW
- GMDN term
- Composite dental impression material
- Device class
- Class II
- Regulation number
- 872.3660
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 92 Gram
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