Amii Implant 401M3013S
by InnoBioSurg Co., Ltd(IBS implant Co., Ltd)
Amii Implant 401M3013S is a Class II device made by InnoBioSurg Co., Ltd(IBS implant Co., Ltd), cleared under FDA 510(k) K220079 on 14 Dec 2022 and listed in FDA GUDID since 23 Apr 2025 (UDI-DI 08809986615053), 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 | Number08809986615053 | Date23 Apr 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK220079 | Date14 Dec 2022 | StatusActive |
Official records
- AccessGUDID record 08809986615053
- FDA 510(k) database K220079
Across registries
- FDA 510(k) K220079 decided 14 Dec 2022 Active
- FDA GUDID UDI-DI 08809986615053 listed 23 Apr 2025 Listed
Timeline
- Cleared FDA 510(k) K220079
- Listed FDA GUDID 08809986615053
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Amii Implant
- Generic name
- Dental implant system
- Model / reference
- 401M3013S
- Primary DI / UDI-DI
- 08809986615053
- 510(k) Number
- FDA product code
- DZE
- GMDN term
- Dental implant system
- Device class
- Class II
- Regulation number
- 872.3640
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Dental implant system.
Other devices from InnoBioSurg Co., Ltd(IBS implant Co., Ltd)
See all devices from InnoBioSurg Co., Ltd(IBS implant Co., Ltd) →