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Final Abutment:TL Abutment - Solid abut.
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref 048.617
Identity
- Trade Name
- SYNOCTA ANGLED ABUTMENTS FDA UDI
- Generic Name
- Dental implant suprastructure, permanent, preformed FDA UDI
- Device Name
- Final Abutment:TL Abutment ( SynOcta / Cementable / Solid abut.) EUDAMEDRN synOcta® Angled Abutment, short, Type A, angled 20 deg., H 5.7mm, Ti FDA UDI
- Model / Reference
- 048.617 EUDAMEDFinal Abutments FDA UDI
- Description
- RN synOcta® Angled Abutment, short, Type A, angled 20 deg., H 5.7mm, Ti FDA UDI
Identifiers
- Catalog Number
- 048.617 FDA UDI
- Primary DI / UDI-DI
- 07630031725325 EUDAMEDFDA UDI
- Basic UDI-DI
- 0763003170006QE EUDAMED
- 510(k) Number
- K994119 FDA UDI
- FDA Product Code
- DZE FDA UDI
- EMDN Code
- P01020101 DENTAL IMPLANTS EUDAMED
- GMDN Term
- Dental implant suprastructure, permanent, preformed FDA UDI
- Models / Variants
- Solid abut. EUDAMEDFDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 872.3640 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Sutures
Yes
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Angle — 20 degree FDA UDI
Final Abutment:TL Abutment - Solid abut. by Institut Straumann AG — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — 3 models
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0763003170006QE | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Institut Straumann AG
- EUDAMED SRN
- CH-MF-000009933
- Authorised Representative
- Etkon GmbH DE-AR-000009335
Sources (2)
- EUDAMED 01a20c21-77a7-401e-934e-b6c38d9312f7 61 fields · synced Jul 14, 2026
- FDA UDI 05ceb209-6574-4c93-86d9-64131a263906 37 fields · synced May 29, 2026