WOODPECKER Surgic Touch
by Guilin Woodpecker Medical Instrument Co., Ltd.
WOODPECKER Surgic Touch is a Class II device made by Guilin Woodpecker Medical Instrument Co., Ltd., cleared under FDA 510(k) K111290 on 18 Nov 2011 and listed in FDA GUDID since 19 Aug 2021 (UDI-DI 06944843601717), active as of 22 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 | Number06944843601717 | Date19 Aug 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK111290 | Date18 Nov 2011 | StatusActive |
Official records
- AccessGUDID record 06944843601717
- FDA 510(k) database K111290
Across registries
- FDA 510(k) K111290 decided 18 Nov 2011 Active
- FDA GUDID UDI-DI 06944843601717 listed 19 Aug 2021 Listed
Timeline
- Cleared FDA 510(k) K111290
- Listed FDA GUDID 06944843601717
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Woodpecker
- Generic name
- Dental ultrasonic surgical system
- Model / reference
- Surgic Touch
- Primary DI / UDI-DI
- 06944843601717
- 510(k) Number
- FDA product code
- DZI
- GMDN term
- Dental ultrasonic surgical system
- Device class
- Class II
- Regulation number
- 872.4120
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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