Patterson® 70496679
by Patterson Dental Supply, Inc.
Patterson® 70496679 is a Class II device made by Patterson Dental Supply, Inc., cleared under FDA 510(k) K882576 on 15 Jul 1988 and listed in FDA GUDID since 30 Apr 2017 (UDI-DI D6620704966790), active as of 24 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 | NumberD6620704966790 | Date30 Apr 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK882576 | Date15 Jul 1988 | StatusActive |
Official records
- FDA 510(k) database K882576
Across registries
- FDA 510(k) K882576 decided 15 Jul 1988 Active
- FDA GUDID UDI-DI D6620704966790 listed 30 Apr 2017 Listed
Timeline
- Cleared FDA 510(k) K882576
- Listed FDA GUDID D6620704966790
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Patterson®
- Generic name
- Composite dental impression material
- Model / Ref / Catalog
- 70496679
- Primary DI / UDI-DI
- D6620704966790
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Composite dental impression material
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
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