FasTouch™ FTPC10

by Via Surgical, Ltd.

FasTouch™ FTPC10 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 21 Aug 2017 (UDI-DI 07290017155111), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07290017155111 UDI-DI	Date21 Aug 2017Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Special	NumberK162252	Date14 Nov 2016Decided	StatusActive

Official records

AccessGUDID record UDI-DI 07290017155111
FDA 510(k) database 510(k) number K162252

Across registries

2 registries list this device

FDA 510(k) K162252 decided 14 Nov 2016 Active
FDA GUDID UDI-DI 07290017155111 listed 21 Aug 2017 Listed

Timeline

2 dated events

14 Nov 2016 Cleared FDA 510(k) K162252
21 Aug 2017 Listed FDA GUDID 07290017155111

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: FasTouch™
Generic name: Endoscopic manual linear stapler
Model / Ref / Catalog: FTPC10

Primary DI / UDI-DI: 07290017155111
510(k) Number: K162252
FDA product code: GDW
GMDN term: Endoscopic manual linear stapler

Device class: Class II
Regulation number: 878.4750
GUDID distribution status: In Commercial Distribution

MRI safety: MR Safe

Size: Outer Diameter — 5 Millimeter
Length — 37 Centimeter

Other devices from Via Surgical, Ltd.

See all devices from Via Surgical, Ltd. →

Properties

Supplied sterile
Single use
Prescription use
Lot / batch number
Expiration date

Other properties (10, all answered No)