FDA UDI
In Commercial Distribution
🇺🇸 United States
Vortex
DI: 00860011853763
·
Model: 17° 4.5*2.0mmH
·
LOUISIANA DENTAL IMPLANT LAB LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Vortex
- Primary DI
- 00860011853763
- Version / Model
- 17° 4.5*2.0mmH
- Company Name
- LOUISIANA DENTAL IMPLANT LAB LLC
- Labeler DUNS
- 077666070
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-09-02
- Public Version
- 1
- Public Version Date
- 2025-09-10
- Public Version Status
- New
- Public Device Record Key
- 4cb89049-3211-463b-a53c-0988a6654c46
Device Description
Angled MUA Abutment 17° 4.5*2.0mmH
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | Dental | 872.3640 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 64312 | Dental prosthesis/implant abutment screw analog, single-use | A device intended to be used as a copy of a dental implant prosthetic screw to attach a dental implant abutment or prosthesis (e.g., crown, bridge) to a dental implant analog in a dental laboratory working model. Some types are referred to as a guide pin, and may be used intraorally to attach an implant coping to the dental implant during an open-tray impression procedure. It is made of metal [e.g., titanium (Ti)] and consists of a rod-like fastener inserted through the abutment/prosthesis. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00860011853763 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K961384 | 000 |