Bosworth Hydrox 0921073
Bosworth Hydrox 0921073 is a Class II device made by Harry J. Bosworth Co., listed in FDA GUDID since 15 Sep 2016 (UDI-DI H66809210731), 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 | NumberH66809210731 | Date15 Sep 2016 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bosworth Hydrox
- Generic name
- Dental pulp-capping material
- Model / Ref / Catalog
- 0921073
- Primary DI / UDI-DI
- H66809210731
- FDA product code
- EJK
- GMDN term
- Dental pulp-capping material
- Device class
- Class II
- Regulation number
- 872.3250
- GUDID distribution status
- In Commercial Distribution
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