Jeil Bone Fixation System 112-080 KIT
Jeil Bone Fixation System 112-080 KIT is a Class II device made by Jeil Medical Corporation, cleared under FDA 510(k) K050669 on 26 May 2005 and listed in FDA GUDID since 18 Jun 2019 (UDI-DI 08806390878029), active as of 23 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 | Number08806390878029 | Date18 Jun 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK050669 | Date26 May 2005 | StatusActive |
Official records
- AccessGUDID record 08806390878029
- FDA 510(k) database K050669
Across registries
- FDA 510(k) K050669 decided 26 May 2005 Active
- FDA GUDID UDI-DI 08806390878029 listed 18 Jun 2019 Listed
Timeline
- Cleared FDA 510(k) K050669
- Listed FDA GUDID 08806390878029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Jeil Bone Fixation System
- Generic name
- Craniofacial fixation plate kit, non-bioabsorbable
- Model / reference
- 112-080 KIT
- Primary DI / UDI-DI
- 08806390878029
- 510(k) Number
- FDA product code
- DZL
- GMDN term
- Craniofacial fixation plate kit, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 872.4880
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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- GBR System SDS-160-030 by Surgident
- SMF TITANIUM (TI) ALLOY BONE SCREWS by Synthes (Usa)
- THE AUTOTAC SYSTEM TITANIUM TACK by BIOHORIZONS IMPLANT SYSTEMS INC.
- SAVE GBR by DENTIS CO., LTD
- Guided Bone Regeneration System by DentalMaster(Xiamen) Medical Technology Co., Ltd.