Patterson® 71217066
by Patterson Dental Supply, Inc.
Patterson® 71217066 is a Class II device made by Patterson Dental Supply, Inc., cleared under FDA 510(k) K012060 on 27 Jul 2001 and listed in FDA GUDID since 8 May 2024 (UDI-DI D6620712170660), 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 | NumberD6620712170660 | Date8 May 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK012060 | Date27 Jul 2001 | StatusActive |
Official records
- FDA 510(k) database K012060
Across registries
- FDA 510(k) K012060 decided 27 Jul 2001 Active
- FDA GUDID UDI-DI D6620712170660 listed 8 May 2024 Listed
Timeline
- Cleared FDA 510(k) K012060
- Listed FDA GUDID D6620712170660
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Patterson®
- Generic name
- Dental ultrasonic surgical system handpiece
- Model / Ref / Catalog
- 71217066
- Primary DI / UDI-DI
- D6620712170660
- 510(k) Number
- FDA product code
- ELC
- GMDN term
- Dental ultrasonic surgical system handpiece
- Device class
- Class II
- Regulation number
- 872.4850
- GUDID distribution status
- In Commercial Distribution
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