Locator 07565
by Zest Anchors, LLC EUDAMEDGUDID
Active
Ref 07565
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08404811Z051EL | Date5 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840481135408 | Date22 May 2026 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- Locator
- Generic Name
- Dental implant kit
- Device Name
- Lodi Surgical Kit
- Model / Reference
- 07565
- Primary DI / UDI-DI
- 00840481135408
- Basic UDI-DI
- 08404811Z051EL
- FDA Product Code
- NDP
- EMDN Code
- L159016 Dental surgery instrument kits, reusable
- GMDN Term
- Dental implant kit
- Device Class
- Class IIa EUDAMEDClass I GUDID
- Regulation Number
- 872.3980
- Medical Purpose
- Accessory Kits for use with the LOCATOR Overdenture Implant (LODI) system.
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class I |
Other devices from Zest Anchors, LLC
Properties
Other properties (8)
- Sterile: No
- Single Use: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No