Rexall UWK
Rexall UWK is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 31 Aug 2020 (UDI-DI 00071031868549), 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 | Number00071031868549 | Date31 Aug 2020 | StatusListed |
Official records
- AccessGUDID record 00071031868549
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rexall
- Generic name
- Dental floss
- Model / reference
- UWK
- Primary DI / UDI-DI
- 00071031868549
- FDA product code
- JES
- GMDN term
- Dental floss
- Device class
- Class I
- Regulation number
- 872.6390
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code JES (Floss, Dental).
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- DENTAL FLOSS CARD by Washburn Laboratories