Woodpecker P56T
by Guilin Woodpecker Medical Instrument Co., Ltd.
Woodpecker P56T is a Class II device made by Guilin Woodpecker Medical Instrument Co., Ltd., cleared under FDA 510(k) K053555 on 21 Aug 2006 and listed in FDA GUDID since 30 Sep 2019 (UDI-DI 06944843600932), 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 | Number06944843600932 | Date30 Sep 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK053555 | Date21 Aug 2006 | StatusActive |
Official records
- AccessGUDID record 06944843600932
- FDA 510(k) database K053555
Across registries
- FDA 510(k) K053555 decided 21 Aug 2006 Active
- FDA GUDID UDI-DI 06944843600932 listed 30 Sep 2019 Listed
Timeline
- Cleared FDA 510(k) K053555
- Listed FDA GUDID 06944843600932
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Woodpecker
- Generic name
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal
- Model / reference
- P56T
- Primary DI / UDI-DI
- 06944843600932
- 510(k) Number
- FDA product code
- ELC
- GMDN term
- Ultrasonic dental scaling/debridement system handpiece tip, periodontal
- Device class
- Class II
- Regulation number
- 872.4850
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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