FasTouch™ SFTP25
FasTouch™ SFTP25 is a Class II device made by Via Surgical, Ltd., cleared under FDA 510(k) K162252 on 14 Nov 2016 and listed in FDA GUDID since 29 Aug 2017 (UDI-DI 07290017155012), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07290017155012 | Date29 Aug 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK162252 | Date14 Nov 2016 | StatusActive |
Official records
- AccessGUDID record 07290017155012
- FDA 510(k) database K162252
Across registries
- FDA 510(k) K162252 decided 14 Nov 2016 Active
- FDA GUDID UDI-DI 07290017155012 listed 29 Aug 2017 Listed
Timeline
- Cleared FDA 510(k) K162252
- Listed FDA GUDID 07290017155012
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- FasTouch™
- Generic name
- Soft-tissue/mesh anchor, non-bioabsorbable
- Model / Ref / Catalog
- SFTP25
- Primary DI / UDI-DI
- 07290017155012
- 510(k) Number
- FDA product code
- GDW
- GMDN term
- Soft-tissue/mesh anchor, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 878.4750
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Length — 37 CentimeterOuter Diameter — 5 Millimeter
Similar devices in this category
Other devices filed under Soft-tissue/mesh anchor, non-bioabsorbable.