Amii Implant 552M5007S
by InnoBioSurg Co., Ltd(IBS implant Co., Ltd)
Amii Implant 552M5007S is a Class II device made by InnoBioSurg Co., Ltd(IBS implant Co., Ltd), cleared under FDA 510(k) K192197 on 28 Apr 2020 and listed in FDA GUDID since 23 Apr 2025 (UDI-DI 08809986616289), 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 | Number08809986616289 | Date23 Apr 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK192197 | Date28 Apr 2020 | StatusActive |
Official records
- AccessGUDID record 08809986616289
- FDA 510(k) database K192197
Across registries
- FDA 510(k) K192197 decided 28 Apr 2020 Active
- FDA GUDID UDI-DI 08809986616289 listed 23 Apr 2025 Listed
Timeline
- Cleared FDA 510(k) K192197
- Listed FDA GUDID 08809986616289
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- Withdrawn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
- 552M5007S
- Primary DI / UDI-DI
- 08809986616289
- 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
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Other devices filed under Dental implant system.
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