Logic /Implex /Expert Nl-Aca-4.5
Logic /Implex /Expert Nl-Aca-4.5 is a Class II device made by Hi-Tec Implants, cleared under FDA 510(k) K941575 on 17 Nov 1994 and listed in FDA GUDID since 8 Jun 2017 (UDI-DI 07290110724108), 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 | Number07290110724108 | Date8 Jun 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK941575 | Date17 Nov 1994 | StatusActive |
Official records
- AccessGUDID record 07290110724108
- FDA 510(k) database K941575
Across registries
- FDA 510(k) K941575 decided 17 Nov 1994 Active
- FDA GUDID UDI-DI 07290110724108 listed 8 Jun 2017 Listed
Timeline
- Cleared FDA 510(k) K941575
- Listed FDA GUDID 07290110724108
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Logic /Implex /Expert
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / Ref / Catalog
- NL-ACA-4.5
- Primary DI / UDI-DI
- 07290110724108
- 510(k) Number
- FDA product code
- NHA
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
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