Straumann Retentive System - Novaloc TiN Abutments Edentulous Abutments
by Institut Straumann SA 55 variants
Listed
Valid until
Not applicable
FDA recalls
None foundDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07630031750365 | Date31 Aug 2020 | StatusListed |
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Straumann Retentive System - Novaloc TiN Abutments
- Generic Name
- Dental implant suprastructure, permanent, preformed
- Model / Ref / Catalog
- Edentulous Abutments, 048.751
- Primary DI / UDI-DI
- 07630031750365
- 510(k) Number
- FDA Product Code
- NHA
- GMDN Term
- Dental implant suprastructure, permanent, preformed
- Device Class
- Class II
- Regulation Number
- 872.3630
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- MRI Safety
- MR Conditional
- Size
- Angle — 15 degreeOuter Diameter — 3.8 MillimeterHeight — 6 Millimeter
Other devices from Institut Straumann SA
Properties
Other properties (9)
- Sterile: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No