FasTouch™

FDA UDI

Class II (US FDA UDI)

by Via Surgical , Ltd.

Identity

Trade Name: FasTouch™ FDA UDI
Generic Name: Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
Device Name: FasTouch™ Permanent Fixation System 25 Permanent Fasteners FDA UDI
Model / Reference: FTP25 FDA UDI
Description: FasTouch™ Permanent Fixation System 25 Permanent Fasteners FDA UDI

Identifiers

Catalog Number: FTP25 FDA UDI
Primary DI / UDI-DI: 07290017155104 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 5 Millimeter FDA UDI
Length — 37 Centimeter 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

Similar devices

Also classified as Soft-tissue/mesh anchor, non-bioabsorbable.

MectaScrew PEEK — Medacta International · Class II
MectaFix CL Fixation Button with Continuous Loop — Medacta International · Class II
HNM MEDICAL — HNM STAINLESS, LLC. · Class II
MectaLock PEEK Suture Anchor — Medacta International · Class II
MectaScrew PEEK — Medacta International · Class II
Anchorsure — DESARROLLO E INVESTIGACION MEDICA ARAGONESA SL · Class II
FiberStitch™ Implant, Reverse Curve with two Polyester Implants and 2-0 FiberWir — T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION · Class II
Heli-FX™ Thoracic EndoAnchor™ System — MEDTRONIC VASCULAR, INC. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Via Surgical , Ltd.

Sources (1)

FDA UDI 385a1ff0-f1e3-423d-a9e2-038459ea90e2 37 fields · synced May 31, 2026