Identity
- Trade Name
- VISION FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- ANTI-ROTATION ABUTMENT FDA UDI
- Model / Reference
- WV-ACA-2 FDA UDI
- Description
- ANTI-ROTATION ABUTMENT FDA UDI
Identifiers
- Catalog Number
- WV-ACA-2 FDA UDI
- Primary DI / UDI-DI
- 07290110724245 FDA UDI
- 510(k) Number
- K941575 FDA UDI
- FDA Product Code
- NHA FDA UDI
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3630 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Vision by Hi-Tec Implants — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure, permanent, preformed.
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- HS/HG Prosthetic System — OSSTEM IMPLANT Co., Ltd. · Class II
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- Diamodent — Diamodent · Class II
- Cemented Abutment — POINTIMPLANT Co., Ltd. · Class II
- GS System — OSSTEM IMPLANT Co., Ltd. · Class II
- Temporary Abutment — Cybermed Inc. · Class II
- EZ Post — Megagen Implant Co. Ltd · Class II
Cleared under the same submission
K941575 also covers:
- HI-TEC IMPLANTS — Hi-Tec Implants
- HI-TEC IMPLANTS — Hi-Tec Implants
- LOGIC — Hi-Tec Implants
- LOGIC — Hi-Tec Implants
- LOGIC — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
- LOGIC /IMPLEX /EXPERT — Hi-Tec Implants
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 II | Pending data |
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Manufacturer
- Manufacturer
- Hi-Tec Implants
Sources (1)
- FDA UDI 60ecea32-2874-4f76-b92f-a12bf4484316 35 fields · synced May 31, 2026