Identity
- Trade Name
- FasTouch™ FDA UDI
- Generic Name
- Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
- Device Name
- Sterile Sample of the FasTouch™ Permanent Fixation System 25 Permanent Fasteners FDA UDI
- Model / Reference
- SFTP25 FDA UDI
- Description
- Sterile Sample of the FasTouch™ Permanent Fixation System 25 Permanent Fasteners FDA UDI
Identifiers
- Catalog Number
- SFTP25 FDA UDI
- Primary DI / UDI-DI
- 07290017155012 FDA UDI
- 510(k) Number
- K162252 FDA UDI
- FDA Product Code
- GDW FDA UDI
- GMDN Term
- Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4750 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 37 Centimeter FDA UDIOuter Diameter — 5 Millimeter FDA UDI
Category: Soft-tissue/mesh anchor, non-bioabsorbable
FasTouch™ by Via Surgical , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Soft-tissue/mesh anchor, non-bioabsorbable.
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Cleared under the same submission
K162252 also covers:
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
- Via Surgical , Ltd.
Sources (1)
- FDA UDI 090b2627-26b1-4129-92e3-c2e7ea4c925a 37 fields · synced Jun 6, 2026