Knit-Pak+ 9007569
by Premier Dental Products Company
Knit-Pak+ 9007569 is a gingival retraction cord (FDA unclassified; FDA product code MVL, Cord, Retraction) made by Premier Dental Products Company, cleared under FDA 510(k) K132526 on 26 Nov 2013 and listed in FDA GUDID since 9 Jan 2024 (UDI-DI 00348783001853), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00348783001853 | Date9 Jan 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK132526 | Date26 Nov 2013 | StatusActive |
Official records
- AccessGUDID record 00348783001853
- FDA 510(k) database K132526
Across registries
- FDA 510(k) K132526 decided 26 Nov 2013 Active
- FDA GUDID UDI-DI 00348783001853 listed 9 Jan 2024 Listed
Timeline
- Cleared FDA 510(k) K132526
- Listed FDA GUDID 00348783001853
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Knit-Pak+
- Generic name
- Gingival retraction cord, non-medicated
- Model / reference
- 9007569
- Primary DI / UDI-DI
- 00348783001853
- 510(k) Number
- FDA product code
- MVL
- GMDN term
- Gingival retraction cord, non-medicated
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
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