Magic Abutment CMAH5005B
by InnoBioSurg Co., Ltd(IBS implant Co., Ltd)
Magic Abutment CMAH5005B is a Class II device made by InnoBioSurg Co., Ltd(IBS implant Co., Ltd), cleared under FDA 510(k) K212517 on 15 Oct 2021 and listed in FDA GUDID since 6 May 2022 (UDI-DI 08800177375794), 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 | Number08800177375794 | Date6 May 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK212517 | Date15 Oct 2021 | StatusActive |
Official records
- AccessGUDID record 08800177375794
- FDA 510(k) database K212517
Across registries
- FDA 510(k) K212517 decided 15 Oct 2021 Active
- FDA GUDID UDI-DI 08800177375794 listed 6 May 2022 Listed
Timeline
- Cleared FDA 510(k) K212517
- Listed FDA GUDID 08800177375794
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Magic Abutment
- Generic name
- Dental implant system
- Model / reference
- CMAH5005B
- Primary DI / UDI-DI
- 08800177375794
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant system
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Safe
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