Identity
- Trade Name
- Locator Core Tool FDA UDI
- Generic Name
- Dental implant system FDA UDI
- Device Name
- Locator Core Tool Places the Locator Abutments and Replacement Males FDA UDI
- Model / Reference
- Locator Core Tool FDA UDI
- Description
- Locator Core Tool Places the Locator Abutments and Replacement Males FDA UDI
Identifiers
- Catalog Number
- 8393 FDA UDI
- Primary DI / UDI-DI
- D785LCT83930 FDA UDI
- FDA Product Code
- DZN FDA UDI
- GMDN Term
- Dental implant system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Locator Core Tool by Oco Biomedical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Oco Biomedical
Sources (1)
- FDA UDI 8a4580c6-d598-477f-8e2a-e33842743cb4 35 fields · synced Jun 8, 2026