ProLube
ProLube is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 1 Sep 2022 (UDI-DI D716PROLUBE1), registry data as of 31 May 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberD716PROLUBE1 | Date1 Sep 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Dental root surface conditioner
- Model / Ref / Catalog
- PROLUBE
- Primary DI / UDI-DI
- D716PROLUBE1
- FDA product code
- EIC
- GMDN term
- Dental root surface conditioner
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
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