Identity
- Trade Name
- Quantum FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- Res-Q TaperLock Abutment 5.0-15° S FDA UDI
- Model / Reference
- 504-050-015 FDA UDI
- Description
- Res-Q TaperLock Abutment 5.0-15° S FDA UDI
Identifiers
- Catalog Number
- 504-050-015 FDA UDI
- Primary DI / UDI-DI
- D8255040500150 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
Single Use
Yes
Implantable
Yes
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Dimensions & Sizes
- Size
- Outer Diameter — 2 Millimeter FDA UDILength — 5 Millimeter FDA UDI
Category: Dental implant suprastructure, permanent, preformed
Introducing the Res-Q TaperLock Abutment, a prefabricated dental implant device designed to provide a permanent intermediate fixture level between a dental implant and the final prosthesis/restoration. With its unique design featuring one or more structural components, including an abutment screw(s), this device is ideal for patients seeking a stable and secure solution.
Similar devices
Also classified as Dental implant suprastructure, permanent, preformed.
- SPARE CAST. SLEEVE FOR — SWEDEN & MARTINA INC · Class II
- HS/HG Prosthetic System — OSSTEM IMPLANT Co., Ltd. · Class II
- DESS dental smart solutions — TERRATS MEDICAL SL. · Class II
- 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
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Quantum Bioengineering, Ltd.
Sources (1)
- FDA UDI b3847c7b-b78b-44d0-a8a3-6a7864370b2f 36 fields · synced Jun 19, 2026