Woodpecker G31
by Guilin Woodpecker Medical Instrument Co., Ltd.
Woodpecker G31 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 20 Oct 2017 (UDI-DI 06944843606996), 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 | Number06944843606996 | Date20 Oct 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK053555 | Date21 Aug 2006 | StatusActive |
Official records
- AccessGUDID record 06944843606996
- FDA 510(k) database K053555
Across registries
- FDA 510(k) K053555 decided 21 Aug 2006 Active
- FDA GUDID UDI-DI 06944843606996 listed 20 Oct 2017 Listed
Timeline
- Cleared FDA 510(k) K053555
- Listed FDA GUDID 06944843606996
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- Withdrawn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, endodontic
- Model / reference
- G31
- Primary DI / UDI-DI
- 06944843606996
- 510(k) Number
- FDA product code
- ELC
- GMDN term
- Ultrasonic dental scaling/debridement system handpiece tip, endodontic
- Device class
- Class II
- Regulation number
- 872.4850
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from Guilin Woodpecker Medical Instrument Co., Ltd.
See all devices from Guilin Woodpecker Medical Instrument Co., Ltd. →