Zuga HCT-430-005
by Zuga Medical, Inc. 2 variants
Zuga HCT-430-005 is a dental implant suprastructure (FDA Class II; FDA product code NHA, Abutment, Implant, Dental, Endosseous) made by Zuga Medical, Inc., cleared under FDA 510(k) K122664 on 30 Apr 2013 and listed in FDA GUDID since 16 Jan 2018 (UDI-DI 00854382006293), 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 | Number00854382006293 | Date16 Jan 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK122664 | Date30 Apr 2013 | StatusActive |
Official records
- AccessGUDID record 00854382006293
- FDA 510(k) database K122664
Across registries
- FDA 510(k) K122664 decided 30 Apr 2013 Active
- FDA GUDID UDI-DI 00854382006293 listed 16 Jan 2018 Listed
Timeline
- Cleared FDA 510(k) K122664
- Listed FDA GUDID 00854382006293
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Zuga
- Generic name
- Dental implant suprastructure, temporary, preformed, single-use
- Model / reference
- HCT-430-005
- Primary DI / UDI-DI
- 00854382006293
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure, temporary, preformed, single-use
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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